DOI: 10.1093/brain/awg086 Brain (2003), 126, 889±907 Hyperfamiliarity for unknown faces after left lateral temporo-occipital venous infarction: a double dissociation with prosopagnosia Patrik Vuilleumier,1,3 Christine Mohr,2 Nathalie Valenza,3 Corinne Wetzel2,3 and Theodor Landis3 London, UK, 2Department of Rehabilitation, University Hospital of Geneva and 3Department of Neurology, University Hospital of Geneva, Geneva, Switzerland Summary Right hemisphere dominance in face processing is well established and unilateral right inferior temporo-occipital damage can result in prosopagnosia. Here, we describe a 21-year-old right-handed woman with acute impairment in face recognition that selectively concerned unfamiliar faces, following a focal left lateral temporo-occipital venous infarct. She was severely impaired in discerning that unknown people seen in everyday life were unfamiliar, although she had no dif®culty recognizing familiar people. Thus, she had no prosopagnosia, but abnormal `hyperfamiliarity' for unknown faces. Her dif®culty was not accompanied by delusions or de®cits in discrimination, identi®cation or memory for faces. Standard neuropsychological testing showed that her recognition of familiar faces was entirely normal. By contrast, her sense of personally knowing faces was severely impaired when unknown faces evoked weak signals of familiarity based on spurious cues, to the extent that she would misattribute fame to faces that were unknown but to which she had been Correspondence to: Dr P. Vuilleumier, MD, Laboratory for Neurology and Imaging of Cognition, Departments of Clinical Neuroscience and Physiology, University Medical Center, 1 rue Michel-Servet, Geneva, Switzerland E-mail: patrik.vuilleumier@medecine.unige.ch incidentally exposed on a prior occasion. Priming experiments also revealed that, unlike normal subjects, she made familiarity judgements without accessing semantic identity representations. Moreover, in face recognition tests, she generally showed bias in that she relied more on right-hemisphere strategies to identify global traits and less on left-hemisphere processes compared with healthy subjects. This case provides novel evidence for a differential contribution of the two hemispheres to face recognition. Hyperfamiliarity for unknown faces might arise from an imbalance between reciprocal hemispheric functions in face recognition, with relative hypoactivation of left hemisphere processes but hyperactivation of right-hemisphere processes for retrieving stored associations about people, linking seen faces to representations of affective and personal relevance. Hence, abnormal bias in attributing some personal meaning to unknown faces could be evoked by spurious signals of familiarity based on irrelevant affective associations in the right hemisphere. Keywords: face recognition; familiarity; prosopagnosia; misidenti®cation; hemispheric laterality Introduction Different disorders of face recognition may follow brain damage. Prosopagnosia, although rare, is the best-known syndrome, and is de®ned as the inability to recognize familiar persons by their face alone (Bodamer, 1947; Damasio et al., 1982; GruÈsser and Landis, 1991). Different forms have been distinguished on the basis of performance in visual tests (Bruyer and Schweich, 1991; GruÈsser and Landis, 1991; McNeil and Warrington, 1991), such as apperceptive cases thought to suffer from a perceptual de®cit in encoding facial traits, and associative cases thought to suffer from the destruction of stored representations of known faces or a Brain 126(4) ã Guarantors of Brain 2003; all rights reserved de®cit in accessing these representations (Bruce and Young, 1986; Burton et al., 1990). Remarkably, some patients with associative prosopagnosia may show evidence of implicit visual recognition of known faces, despite a complete lack of familiarity with such faces (Bauer, 1984). This suggests that the subjective experience of recognizing a face may involve not only adequate perceptual processing and activation of internal representations of face traits, but access to more complex associations stored in memory that pertain to the identity of a known person (Damasio et al., 1990; Schreiber et al., 1991). Accordingly, the perception of a familiar face Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 1Institute of Cognitive Neuroscience, University College 890 P. Vuilleumier et al. Table 1 General neuropsychological assessment Test Visual object recognition Poppelreuter overlapping shapes Montreal±Toulouse Agnosia Test Object parts Colour test Executive functions Verbal letter ¯uency (2 min) Verbal category ¯uency (2 min) Visual design ¯uency (3 min) Trail Making Test A Trail Making Test B Luria graphic sequences Luria gesture sequences Colour-Word Stroop D2 Test of sustained attention Correct targets cancelled Errors Memory Digit verbal span Corsi visuospatial span Rey word list learning Immediate recall 1 Immediate recall 2 Immediate recall 3 Immediate recall 4 Immediate recall 5 Delayed recall Delayed recognition Rey visual shape learning Immediate recall 1 Immediate recall 2 Immediate recall 3 Immediate recall 4 Immediate recall 5 Delayed recall Delayed recognition Maximum or minimum score * 31 43 89 198 12 4 4 /44** /44 /90 /200 /12 /4 /4 Centile 10±50 8 8 8 6 /8 /8 /8 /6 20 Right hand, 15 Left hand, 15 /20 /15 /15 5 20 20 18 /5 /20 /20 /18 32 39 32 25 s 77 s 15 5 48 Min. = 25 Min. = 27 Min. = 27 Max. = 34 Max. = 85 /15 /5 /49 404 4 /700 5 7 ** 12 14 15 15 15 14 15 /15 /15 /15 /15 /15 /15 /15 5 7 13 13 15 15 15 /15 /15 /15 /15 /15 /15 /15 Centile 10 *Norms are based on the Standardized Geneva Hospital Neuropsychology Battery (unpublished) or published data (Spreen and Strauss, 1991; Benton et al., 1994). Abnormal performance in patient J. R. is indicated by ** (centile 10); otherwise, performance was within the normal range (centile 50). Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Language Object naming Boston Naming 1 Boston Naming 2 ExaDE Bachy±Langedock test Word reading Oral spelling Writing Calculation Ideomotor and constructional praxis Right hand Left hand Orofacial Drawing Body schema Culver right±left orientation test Benton ®nger agnosia test Patient J. R. Hyperfamiliarity for unknown faces such disorders is that they involve a disturbance in the activation of affective and semantic associations about known people, triggered by inappropriate faces and/or other irrelevant cues (Ellis and Young, 1990). Thus, subjective appraisal of familiarity is speci®cally altered but identi®cation of known faces can be preserved (Ellis and Young, 1990; Sno and Linszen, 1990), although memory and perceptual processing of faces are often reported to be also impaired (Young et al., 1990). A wide variety of lesions has been reported in such patients, including unilateral right (Young et al., 1990), bilateral (Burgess et al., 1996) and diffuse (FoÈrstl et al., 1991) cerebral damage. Unlike these cases, our patient had a very focal cortical lesion and she showed no delusion and no de®cit in face perception or face memory, even during the acute post-onset stage. Detailed neuropsychological tests were conducted to document her performance at various levels in the face recognition system and to investigate the possible factors associated with her hyperfamiliarity for unknown faces. Case history J. R. was a 21-year-old right-handed (Old®eld's laterality index 100%) female student without previous neurological or psychiatric history. She was born in Switzerland and spent her childhood in Geneva. Following normal education in primary school, she obtained her high school diploma and started studying the history of art and linguistics at university. She was very keen on theatre plays and artistic paintings. She had never experienced any dif®culty in person recognition or memory in the past. J. R. was admitted to hospital because of sudden headaches, nausea and a generalized tonic±clonic seizure. She had no neurological de®cit, in particular no visual ®eld defect, and no language disturbance. Detailed neuropsychological assessment was performed in the ®rst and third weeks after onset. There was only mild word-®nding dif®culty in the ®rst testing session that resolved on the second session, and slightly impaired short-term verbal memory (Table 1). Verbal and visual learning, frontal executive and basic visuoperceptive functions were intact. Brain CT revealed a haemorrhagic infarct in the left lateral temporo-occipital region in the territory of the vein of LabbeÂ, caused by thrombosis of the left transverse and sigmoid venous sinuses, and it was con®rmed by conventional arteriography and MRI (Fig. 1). There was no other brain lesion. A hereditary defect in antithrombin III was diagnosed. After local intravenous thrombolysis, oral warfarin and phenytoin were started; the medical course was favourable, with partial sinus recanalization on magnetic resonance angiography 10 days later. EEG showed slow waves and occasional sharp waves in the left posterior regions during the ®rst week, with rapid improvement and only moderate slowing during the second week. Repeated EEGs were normal afterwards. In hospital, J. R. had no dif®culty recognizing known people and learning new faces but spontaneously complained Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 generally triggers the activation of a rich assemblage of information concerning unique biographical details, past contextual episodes, affective relevance, and so on, which all participate in the subjective recollective experience associated with face recognition (Damasio et al., 1990; Van Lancker, 1991). However, such associative components of face recognition, beyond purely visual perceptual processing, remain largely unknown. While prosopagnosia is most often associated with bilateral ischaemic lesions in the territory of the posterior cerebral arteries, unilateral damage to the inferior temporo-occipital cortex (areas 20, 21 and 37) in the right hemisphere appears suf®cient to cause associative prosopagnosia, with complete loss of familiarity for known faces despite relatively intact perception and discrimination abilities (Landis et al., 1986, 1988; De Renzi et al., 1994). However, some authors have suggested that bilateral damage may be mandatory (Damasio et al., 1982) or lead to more profound de®cits (Rhodes, 1985). It remains uncertain (i) whether right hemisphere function is crucial for recognizing familiarity, besides its superior role in visual facial analysis; and (ii) whether the left hemisphere makes any useful contribution to face recognition in humans. No case of prosopagnosia or any other selective disorder of face recognition subsequent to a unilateral left hemisphere lesion in a right-handed subject has yet been reported. Here we report a young woman who presented with a peculiar disorder of face recognition following a lesion restricted to the lateral temporo-occipital junction of the left hemisphere due to a venous infarction. The patient exhibited a selective de®cit in judging the familiarity of unknown faces, but she had no dif®culty discriminating and recognizing known faces, and showed no delusion, confabulation or any other general cognitive impairment. Such a de®cit has not been described previously as an isolated disturbance, and constitutes double dissociation with respect to defective recognition of familiarity for known faces in associative prosopagnosia. This patient provides unique insights into the left hemisphere's contribution to face processing and the data suggest a reciprocal function of the two hemispheres in associative recognition processes that bestow an experience of personal familiarity on seen faces. It also exempli®es the unique value of lesions situated outside common vascular territories in revealing novel brain±behaviour relationships, as historically shown for other rare de®cits due to tumours (Trescher and Ford, 1937) or venous infarctions (Zihl et al., 1983). The false familiarity with faces presented by our patient was very different from disorders of familiarity associated with delusional misidenti®cations, such as Capgras syndrome, in which the patient believes that a familiar person has been replaced by a disguised impostor, or FreÂgoli syndrome, in which the patient believes that a known person has disguised himself as another person (Ellis and Young, 1990; Young et al., 1990). These psychiatric disorders may occasionally follow brain damage (Young et al., 1990; Signer, 1994). It has been suggested that a critical aspect of 891 892 P. Vuilleumier et al. about continuously experiencing erroneous familiarity for unknown people's faces. Her errors concerned other patients, visitors and hospital staff, and greatly embarrassed her. She often engaged in effortful memory searching to decide that she was mistaken, or had to ask the person whether they knew each other. Such errors were very frequent during the ®rst 3 weeks (almost all encounters during the ®rst week and more than half of new encounters up to 3 weeks, according to the patient) then gradually decreased. These errors were still frequent during the time of our investigations, and persisted to a lesser degree after more than 1 year of follow-up. Initially every person who entered her hospital room was familiar to her, she thought she knew him or her, and she would smile at him or her, expecting the person to sit next to her bed and chat with her. It was quite frightening to her that many visitors did not notice her and continued towards her roommate, an elderly woman she knew she had never met. At these moments she tried to ®gure out where she knew these people from, and would engage in lengthy memory searches. Was it the father of a school friend she had met once? A person seen in the news? A writer seen in a newspaper? A man met at a recent party? She rapidly became suspicious about her own perception of intimate familiarity with these people, but was still often initially convinced that she knew a face at ®rst sight despite clear evidence to the contrary. On questioning, she admitted that during the ®rst 48 h she might also have experienced on a few occasions a similar feeling that the voices of these unknown persons sounded familiar. However, this feeling of false voice familiarity was much weaker than that of face familiarity; it was always accompanied by simultaneous false familiarity for the face and then faded rapidly. She never experienced any dif®culty recognizing voices on the telephone or radio. During the ®rst grand round on the ward (4 days after admission), J. R. greeted one of the authors (T. L.) by using the familiar form of personal pronoun (tu, unusual in French with an unknown physician), smiling at him as if he was somebody known to her, though she could not retrieve his name right away. Realizing her mistake, she excused herself and said: `Sorry, you must be the professor, it got me again, I cannot trust my own perceptions. When you entered this door I thought I knew you well, well enough so that you would Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Fig. 1 Brain MRI of the patient 10 days after stroke (A±D) and 1 year later (E±F). (A) T2-weighted coronal and (B) T1-weighted sagittal images showing haemorrhagic infarction in the posterior middle and inferior temporal gyri of the left hemisphere, close to the temporooccipital junction, and in the paraventricular occipital white matter. (C, D) Corresponding anatomical templates using the method of Damasio and Damasio (1989). The acute lesion was centred on Brodmann areas 37, 21 and 20. (E) In the chronic stage, T1-weighted coronal images show a focal cystic lesion in the same area. (F) Corresponding anatomical templates, showing that persistent damage is centred on the middle temporal gyrus. Hyperfamiliarity for unknown faces 893 Table 2 General face perception abilities Controls: cut-off (mean 6 SD) 49/54 6 : 45 39 (45.4 63.9) 8 : 00 (5 : 33 6 74 s) 29/30 30/30 24/24 9/9 10/10 12/12 20/20 30/30 12/12 24 (24.0) 9 (9.0) 10 (10.0) 12 (12.0) 18 (19.6) 26 (29.1) 11 (11.7) 43/48 23/24 20/24 39 (46.2) NA NA 23/24 20/24 23/24 42/42 18/24 19/24 15 (20.5) 19 (23.0) 40 (40.3 6 0.8) 9 (12.5 6 3.2) 19 (20.8 61.5) 100/110 1/50 564 ms 97 (101 6 4.0) 3 (2.0 61.0) 604 (6 225) ms In all tests, the patient's performance was compared with that of normal subjects of similar age and education level, as available from published norms (Bruyer and Schweich, 1991; Benton et al., 1994) or from our own data. embrace me and call me by my ®rst name. Apparently we do not know each other, but I still have that feeling of having met you many times'. She also explained: `My eyes are caught by someone's face; I have the strong feeling of knowing him or her without being able to place him or her ¼ I have the feeling we have met in some place or talked together, but I cannot ®gure out where or when, or what we talked about. This happened to me occasionally before, as to everyone I suppose, but now it is present all the time and with everybody. This occurred with many nurses, I often asked them if we were together at school, or if we were living in the same neighbourhood. Also, I thought I had already met with some of the doctors, long before my illness, yet I don't know when'. By contrast, correct recognition was con®dent and associated with immediate retrieval of a speci®c identity. `When I truly recognize someone, I have no doubt: I just know who the person is. It is more automatic, more natural. When I am not sure, I give a smile or say hello, I wait and see'. In the initial phase of her illness she said that the inability to recognize unfamiliarity was practically ubiquitous, concerned most newly encountered people, and was independent of the surroundings within the hospital, whereas her ability to recognize truly familiar persons was never impaired. However, after discharge a few weeks later, it appeared that her errors with unfamiliar faces were in¯uenced by the situational context. Familiarity errors were less common when she was walking in the street or using public transport, but increased speci®cally when she was on the university campus, in her neighbourhood or visiting the hospital during follow-up. J. R. never misidenti®ed a person for another and never thought people were disguised. Her familiarity errors with unknown faces were quite dramatic during the ®rst 2 weeks and then decreased gradually over a period of months, but were still present after 1 year of follow-up (10% of new faces, in the patient's estimation). Subsequent MRI scans 6 and 12 months after onset showed considerable shrinking of the lesion, with a chronic infarct centred on the posterior middle temporal gyrus (Fig. 1E and F). In summary, this striking disturbance in which unknown faces are appraised as familiarity from unknown faces constitutes a novel clinical phenomenon, hitherto never reported, caused by an unusual lesion outside the common Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Benton matching test (Benton et al., 1994) Total correct Total time (min : s) Mooney face closure test (Lansdell, 1968) Male/female discrimination Young/old discrimination Bruyer and Schweich battery (Bruyer and Schweich, 1991) subtests 1. Face/non-face decision 2. Matching isolated facial features 3. Matching identity across different view 4. Matching across different expressions 5. Gender classi®cation 6. Age classi®cation 7. Recognition of facial expressions 8. Familiarity decision Total correct Famous faces correctly recognized Unknown faces correctly rejected 9. Recognition of famous faces Semantic information Naming: spontaneous Naming: cued Eye-gaze direction (Campbell et al., 1990) Recognition of caricatures Disguise Task (Young et al., 1990) Actors Task Total correct False alarms on distractors Mean reaction time (correct responses) Patient J. R.: raw score 894 P. Vuilleumier et al. Table 3 General memory abilities Controls: cut-off (mean 6 SD) 34/40 4/60 30 4.19 0.43 (34.3 6 5.1) (3.1 6 2.8) 22 (31.1 6 5.5) (2.8 6 0.6) (0.31 6 0.2) 35/40 0/60 35 6.66 1.47 (37.8 6 2.8) (0.8 6 0.8) 28 (37.0 6 2.9) (3.7 6 0.4) (0.34 6 0.32) 30/36; percentile 60 24/24; percentile >99 16/24; percentile 10 18 (28) 14 (19) 15 (19) 87/115 43 16 28 44 42 41 80 (99) 39 (43) 20 (25) 26 (30) NA; max. 45 NA; max. 45 NA; max. 45 In all tests, the patient's performance was compared with that of normal subjects of similar age and education level, as available from published norms (Baddeley et al., 1994; Bindschaedler et al., 1995) or our own data. arterial territories involved in ischaemic strokes. It provides a unique piece of evidence for an important function of the left cerebral hemisphere in the recognition of faces and in mechanisms of familiarity. Below, we report our examination of various aspects of face processing in J. R. using a large battery of standard tasks that are commonly used in prosopagnosia, and a number of ad hoc experiments. General face processing and memory abilities All the following experiments were performed during the third week after stroke to test for the presence of prosopagnosia, i.e. an impairment in the ability to discriminate and remember familiar faces. Several standardized tests were given to probe (i) basic face perception abilities (Table 2) and (ii) general memory abilities for faces, people and other complex visual material (Table 3). As indicated in Table 2, testing for general face perception abilities comprised a battery of nine subtests assessing separate recognition processes, including a familiarity decision task that required classi®cation of a series of faces as famous or unknown [the Bruyer and Schweich battery (Bruyer and Schweich, 1991)], a test of con®gurational facial organization (Lansdell, 1968), the discrimination of individual faces in different views (Benton et al., 1994), and the perception of gaze direction (Campbell et al., 1990). A few other special tests assessed the identi®cation of faces with an unusual appearance. Recognition of caricatures (e.g. of politicians) was examined because it has been suggested that memory representations of familiar faces may exaggerate distinctive physiognomic features, as do caricatures (Rhodes et al., 1987), and a defect in extracting such distinctive features might conceivably induce abnormal familiarity with unknown people. Also, we used a disguise task (Young et al., 1990) that required matching unfamiliar faces masked by various disguises (e.g. glasses or a false beard), and a similar task, the Actor Task, that required recognition of famous actors in different roles (e.g. with different make-up or age). Patients with delusional misidenti®cation are particularly impaired on such tasks, whereas they have no dif®culty recognizing undisguised faces (Young et al., 1990). General memory abilities were assessed with a recognition memory test for faces and words (Bindschaedler et al., 1996), the Doors and People Test (Baddeley et al., 1994), and structured questionnaires assessing semantic knowledge about familiar people and celebrities (Ellis et al., 1989; Kapur et al., 1992), adapted and standardized for the Swiss population (Bindschaedler et al., 1995). Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Recognition memory test (Bindschaedler et al., 1996) 1. Faces Hits (H) False alarms (FA) Total correct (H ± FA) Discrimination (d¢) Response bias (C) 2. Words Hits (H) False alarms (FA) Total correct (H ± FA) Discrimination (d¢) Response bias (C) Doors and People Test (Baddeley et al., 1994) People Doors Names Semantic knowledge of people (Kapur et al., 1992; Bindschaedler et al., 1995) Dead±Alive People test: total score 1. Dead/alive decision 2. Date of death 3. Mode of death 4. Profession 5. Achievement 6. Nationality Patient J. R.: raw score Hyperfamiliarity for unknown faces Results Global and featural visual processing of faces Several additional tests were designed to examine face recognition beyond the basic perceptual stages. All these tests were administered between the fourth and eighth weeks after onset. During this period, the patient was still making frequent familiarity errors with unknown faces in everyday life, and control MRI scans demonstrated that a chronic lesion restricted to the middle temporal gyrus persisted up to 1 year after onset (Fig. 1E and F). The following experiments probed speci®cally for an impairment in encoding local compared with global traits in faces. It is known that the left hemisphere is preferentially involved in parsing local features, while the right hemisphere is more concerned with global con®gurational traits (e.g. Hillger and Koenig, 1991; Tanaka and Farah, 1993; Rossion et al., 2000). As shown by Yarbus (1967), visual exploration of faces is driven strongly by internal parts, such as the eyes, nose and mouth. These internal parts are more important than external features or whole contours in the recognition of known faces, whereas both internal and external features are equally important for unfamiliar faces (Ellis et al., 1979; Young et al., 1985b). Left hemisphere damage might have disrupted the processing of local features, leading to false recognition based on the predominance of right-hemispheric processing of global or external traits. The three tasks described below (Inverted Face, Face Parts, and Altered Face) were used to compare the roles of parts and wholes in face recognition and familiarity judgements. Whenever possible, performance was measured not only by accuracy and error rates, but also by signal detection measures of discrimination and response bias. Indeed, J. R.'s problem involved a false feeling of familiarity for persons without real personal meaning, i.e. she made false alarms and accepted new faces as already known, but did not fail to recognize previously known or famous faces (i.e. she was not prosopagnosic). Signal detection measures allowed us to take the whole of her decision behaviour into account, by calculating d¢ values for her visual discrimination sensitivity and C values for her personal response criteria strategy (Green and Swets, 1966). At a d¢ value of zero it can be assumed that the observer cannot distinguish between a signal and background noise. Increasing d¢ values indicate that the signal is more salient and more easily recognized. On the other hand, a low C value indicates that the observer accepts less salient signals as possible hits, and thus makes errors but also achieves a high rate of correct answers. High C values indicate a more strict decision threshold, with fewer mistakes but also a lower hit rate. To compare J. R. with normal subjects, we calculated the con®dence intervals for d¢ and C values from the means and standard deviations obtained for the normal subjects. As in the method of Hirsig (1998), we used t values instead of Z values because of the small control sample (e.g. six or eight subjects). Values of t corresponding to the appropriate number of degrees of freedom (d.f.) were taken from tables provided by Hirsig (1998), with the 95% level set at t = 2.57 for six subjects and t = 2.37 for eight subjects. We calculated ®rst the estimated standard deviation (s = s/Öd.f., where s is the standard deviation of the control sample), and then the con®dence interval for the mean (CI = m 6 t95% 3 s, where m is the mean value of the control sample). This con®dence interval is the range of values within which 95% of the general population would be likely to lie, given the sample. We assumed that the performance of our patient was abnormal if it was outside this interval. Inverted face task This test compared recognition of upright and upside-down faces. Extraction of salient local features is more important for upside-down than for upright presentation (Yin, 1969). Inversion can remove the right hemisphere superiority normally found with upright faces (Hillger and Koenig, 1991). Thus, defective encoding of local features should disturb recognition of inverted faces disproportionately. In this task, black-and-white photographs of 20 unknown upright faces were shown sequentially for study (1 s each). Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 The patient's performance in these standardized tests was well within the normal range (Table 2). She had no impairment in matching unfamiliar faces or identifying familiar faces (i.e. no prosopagnosia). She made no misidenti®cation of known or unknown faces. Caricatures, faces in disguise and actors were all recognized correctly. Similarly, her scores in the visual recognition memory test were in the normal range (Table 3). False alarms were not increased in the face memory task (Table 3), and signal detection measures (Bindschaedler et al., 1996) showed excellent discrimination ability (high value of d¢, corresponding to ef®cient discrimination of signal from noise), without a signi®cant response bias in making recognition judgements compared with the normal range (loose criteria for familiarity decisions correspond to small or even negative values of C; see below). Note, however, that her response criteria appeared to be higher for words than faces, unlike normal controls (Table 3). Finally, retrieval of biographical information about well-known people in the Dead±Alive test (Kapur et al., 1992) did not differ from results for normal subjects (Table 3); her slightly poorer performance on dates of death was probably due to the patient's young age (Bindschaedler et al., 1995). Structured interviews with the patient and her family (Ellis et al., 1989) revealed no loss in semantic knowledge about close relatives. From these tests and the clinical picture of the patient, who never mistook for a stranger somebody she knew or failed to name a person really familiar to her, it can be concluded that she was not prosopagnosic and had no basic perceptual dif®culties with faces. Therefore, her dif®culties with face familiarity must have had an origin other than a de®cit in the basic visual analysis of faces or memory. 895 896 P. Vuilleumier et al. Table 4 Recognition of inverted and upright faces No. of `old' responses J. R. (controls) d¢ value Faces Correct False alarms Inverted Upright 11 (12.8 6 1.8) 10 (12.5 6 1.3) 8 (6.5 6 1.2) 1 (3.5 6 1.9) .C value J. R Controls 95% CI J. R. Controls 95% CI 0.4 1.6 0.6 to 1.0 0.9 to 1.7 0.1 0.8 ±0.1 to 0.2 0.1 to 0.5 Controls were eight age- and education-matched normal subjects (®ve females and three males, mean age 27.5 years). Signi®cant differences between patient and controls are indicated in bold. CI = con®dence interval. Results The number of correct `old' responses made by J. R. was within the controls' range for both inverted and upright faces, but she tended to produce a greater proportion of incorrect `old' responses for inverted faces (Table 4). Inversion decreased face recognition sensitivity (d¢) in J. R. to a greater degree than expected from the decrease in control subjects. Her response criterion (C) did not differ from that of controls for inverted faces, but was more conservative for upright faces. Her mean reaction time for correct responses (1493 ms) was comparable to that of controls (1331 6 574 ms). This pattern would be consistent with a mild dif®culty arising when recognition must rely more on the left hemisphere for processing internal facial features. Face parts task This task compared recognition of facial parts and wholes in separate phases. We used two versions (given a few days apart), which used either famous or unknown faces. Each version employed 24 black-and-white photographs of faces that were cut out into four parts (hair, eyes, nose and mouth) (Fig. 2A), yielding a total of 96 stimuli. In the study phase, 12 full target faces were presented on a computer screen (5 s each). Two test phases immediately followed. First, all 48 parts from the target faces were presented in random order mixed with 48 distractor parts from the other 12 faces. Subjects made familiarity decisions (old/new) with a key press. Stimuli remained on the screen until there was a response. Immediately afterwards, a second test phase assessed the recognition of whole faces. All target and distractor faces were presented once again, but now in wholes. Subjects made familiarity decisions (old/new) as in the ®rst test. Response time and accuracy were recorded. Results J. R. showed no obvious de®cit in recognizing single facial features from either famous or unknown people (Table 5). Signal detection values con®rmed that her discrimination sensitivity for facial parts and wholes was within or even above the normal controls' range in all conditions. However, she made more incorrect `old' judgements on `new' nose and mouth parts [c2(1) = 4.0, P = 0.04] and used looser response criteria for these parts compared with normal subjects. Her mean reaction time for correct responses (1684 ms) was similar to that of controls (1651 6 813 ms). These data suggest that, despite her well-preserved visual discrimination abilities, J. R. might have experienced some uncertainty when using only local feature information as the basis for the recognition of face familiarity, especially when such facial features were new. Altered face task This task pitted recognition of parts and wholes against each other within the same stimulus. It consisted of a continuous recognition memory test in which 60 faces recurred once each, intermingled in random order with 60 distractors (180 trials in total). Four additional faces served as a buffer at the beginning of the test. All faces were from unknown persons. Intervals from ®rst presentation to repetition varied between 10 and 60 intervening stimuli (mean 34). On repetition trials, the target faces were either unchanged or altered at the internal (eyes, mouth), external (hair) or global (whole face) level (12 trials in each condition; Fig. 2B). All stimuli were shown sequentially on a computer screen (1 s). Subjects were required to indicate whether the face of any given person was repeated or seen for the ®rst time by pressing one of two keys (old/new). Results Table 6 shows that J. R. recognized the recurrence of unchanged faces as well as normal subjects did [75 versus 83%; c2(1) = 0.09, P = 0.75] and made fewer false alarms to new faces (19 versus 29%). The rate of `old' response to faces that were altered on repetition trials was signi®cantly affected by the type of change, both in J. R. [c2(3) = 15.6, P = 0.001] and in normal subjects [c2(3) = 8.0, P = 0.050]. Such `old' Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Then, the same (old) faces and an equivalent number of new faces were brie¯y presented upside-down (500 ms) in random order. Familiarity (old/new) was indicated for each face by a key press. In a third phase, the old faces and another set of new distractors were presented in the normal upright position using the same procedure. Response time and accuracy were recorded. Hyperfamiliarity for unknown faces 897 responses to altered faces were lower in J. R. than in normal subjects when the hair was changed (25 versus 47%), but higher when the eyes or mouth were changed (75±83 versus 54±67%), and identical when the whole face was changed globally (58%). This pattern would be expected if J. R. recognized familiarity by relying more on external and global components of faces, and less on internal features (eyes and mouth) compared with normal subjects. The total difference between external and internal changes was signi®cant in J. R. (10 versus 19 faces recognized out of 24, P = 0.002, Fisher's test) but not in controls (mean 12.6 versus 14.5 recognized, P = 0.15). Her mean reaction time for correct responses (1382 ms) was also similar to that of controls (1472 6 667 ms). Chimaeric face task The above results are partly consistent with an impairment of face processing involving the left hemisphere, possibly resulting in defective encoding of internal features and abnormal reliance on global components. However, all the preceding tests examined judgements of familiarity in conditions in which the patient was required Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Fig. 2 Examples of stimuli used to test global and local visual processing. (A) Face parts. Unfamiliar whole faces were presented in the study phase and their parts (hair, eyes, nose, mouth) were presented in a subsequent recognition test. A similar task employed famous faces. (B) Altered faces. From ®rst presentation (upper row) to repetition (lower row), target faces were either unchanged or altered at the global (whole face), external (hair) or internal (eyes, mouth) level. (C) Chimaeric faces. Three kinds of chimaera were constructed (the French actress Isabelle Adjani is shown as an example), using the global contour and hair from a known face but changing the eyes or mouth (inner chimaeras), or vice versa (outer chimaeras). The original face itself was not presented, and a given individual appeared only once. For the patient, similar chimaeras were constructed using both famous faces and faces of relatives. 898 P. Vuilleumier et al. Table 5 Recognition of facial parts and wholes No. of old responses J. R. (controls) C value J. R. Controls 95% CI J. R. Controls 95% CI 1 (3.3 6 2.1) 2 (2.3 6 1.6) 6 (3 6 1.5) 4 (2.5 6 1.6) 0 (0.5 6 0.8) 2.4 1.2 0.7 0.9 4.7 0.8 to 2.0 0.7 to 2.1 0.2 to 1.1 0.4 to 1.5 3.4 to 4.1 0.2 0.4 ±0.3 0.0 0.0 ±0.4 to 0.5 0.0 to 0.8 0.0 to 0.9 0.1 to 0.9 ±0.4 to 0.5 0 (0.5 6 0.5) 0 (0.8 6 0.5) 1 (2.4 6 1.2) 0 (2.5 6 1.8) 0 (0) 3.7 4.7 2.1 4.7 4.7 2.3 to 4.1 2.0 to 3.1 0.2 to 1.8 1.1 to 2.9 4.7 0.5 0.0 0.4 0.0 0.0 0.0 to 0.5 0.0 to 0.6 0.2 to 0.6 ±0.3 to 0.2 0.0 Correct False alarms 10 (8.8 6 1.3) 7 (7.3 6 1.3) 9 (5.3 6 1.9) 8 (6 6 1.7) 12 (11.5 6 0.5) 11 (10.5 6 1.2) 12 (9.8 6 1.4) 9 (6.4 6 1.8) 12 (10.0 6 1.3) 12 (12) Controls were eight age- and education-matched normal subjects (®ve females and three males, mean age 27.5 years). Signi®cant differences between patient and controls are indicated in bold. CI = con®dence interval. Table 6 Recognition of altered faces No. of `old' responses Repeated faces Unchanged Global change Hair change Eyes change Mouth change New faces J. R. Controls (mean 6 SD) 9/12 7/12 3/12 10/12 9/12 23/120 10 6 0.8 7 6 2.7 5.6 6 1.8 8 6 1.7 6.5 6 2.6 34.5 6 15.4 Controls were eight age- and education-matched normal subjects (®ve females and three males, mean age 27.5 years). to recognize whether she had already seen a given face rather than judge whether any particular face was from a person known to her. Critically, her disturbing feeling of abnormal familiarity with strangers in real life was associated not only with an impression of past occurrence, but also with some aspect of personal relevance and more intimate knowledge. Therefore, if preferential encoding of global and external components at the expense of internal features were suf®cient to induce such a false familiarity, our patient would be expected to judge mistakenly that she knew chimaeric faces who have familiar external features and incorrect internal features, but not faces with the reverse chimaeric manipulation (i.e. familiar internal and unfamiliar external features). In this task, we constructed chimaeric faces from photographs of 14 relatives of the patient, 14 famous actors and 21 unknown people. Seven faces in each category served as unchanged stimuli, while the others were employed for chimaeric stimuli. There were three possible chimaeras for both relatives and famous people (Fig. 2C): outer contour chimaeras (global contour and hair from an unknown face with eyes and mouth from a known face); inner eyes chimaeras (unknown eyes in known face contours); and inner mouth chimaeras (unknown mouth in known face). Each individual face and parts were used only once, resulting in 63 stimuli. All faces were projected brie¯y (800 ms) on a computer screen and familiarity judgements (known/unknown) were made by key press as quickly as possible. Controls were tested with unknown and famous faces only. Results J. R. recognized real non-chimaeric faces normally, and showed no increase in false alarms or response times to chimaeric faces with familiar global contours (Table 7). There was no difference for famous faces known through the mass media and faces of personally known relatives. This indicates that J. R. could still correctly assess the familiarity of faces using both internal and global features within a single face, and did not mistakenly recognize a face with familiar global features as a known face. Therefore, although the preceding experiments suggest that the patient tended to rely more on face-processing abilities subserved by the right than the left hemisphere, with the patient showing better encoding of external than internal features when the recognition of familiarity or a previous encounter with a face was required (e.g. in the inverted face and altered face tasks), this visual bias did not seem suf®cient to induce a false feeling of personal acquaintance with unknown faces, as otherwise exhibited by J. R. in her everyday life. Associative and semantic processes in face recognition The previous series of experiments showed that visual facial processing was well preserved in J. R. overall. Preferential Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Unknown faces Hair Eyes Nose Mouth Whole Famous faces Hair Eyes Nose Mouth Whole d¢ value Hyperfamiliarity for unknown faces Table 7 Recognition of chimaeric faces Table 8 Misattribution of fame No. of `known' responses No. of `fame' responses J. R. J. R. Controls (mean 6 SD) 11/20 3/20 16/20 12.7 6 2.4 2.2 6 3.3 6.3 6 0.5 11/20 1/20 6/20 16.2 6 0.8 1.7 6 0.5 5.3 6 1.2 Controls (mean 6 SD) 2 061 6 1 1 0 661 161 161 0 7 0 0 0 1029 ms (max. = 7)* (max. = 7)* (max. = 7)* (max. = 7)* 1131 6 226 ms Controls were four age- and education-matched normal subjects (four females, mean age 27.4 years). *Controls were tested only with unknown and famous faces, whereas J. R. was also tested with faces of family relatives. engagement of the right hemisphere for global visual analysis of faces, with relatively de®cient encoding of local features in the left hemisphere, could not fully account for her abnormal feeling of personally knowing new faces. We therefore designed the next series of experiments (performed 7 and 8 weeks after onset) to investigate whether impaired processing of faces in the left hemisphere might affect a stage of stimulus analysis beyond purely visual perceptual encoding, at the level where associations with representations stored in memory are formed and used to access speci®c information about personal identity. False fame and prior face exposure Failure to activate appropriate semantic representations can lead to false recognition and misattribution of familiarity when retrieval of such information is necessary in order to recognize (or reject) the source of subjective familiarity induced by erroneous cues (Jacoby et al., 1989a; Whittlesea and Williams, 1998). In normal people, previous exposure to unknown names (Jacoby et al., 1989b) or unknown faces (Bartlett et al., 1991) can generate such a feeling of familiarity and induce erroneous judgements of celebrity, especially when the individual fails to recollect the context associated with prior exposure. We examined whether J. R. would be abnormally prone to false familiarity effects under such conditions. In this task, a series of 60 faces were shown sequentially and had to be judged as famous or unknown. No speci®c biographical information or name was required. The stimuli included 20 people with real but modest fame (e.g. minor local politicians, second-rank artists etc.), together with 20 unknown people who had been presented only once as distractors in a previous test (old lures), and 20 other Faces Real fame New lures Old lures Names Real fame New lures Old lures Controls were six age- and education-matched normal subjects (®ve females and one male, mean age 25.0 6 3.7 years). The bold ®gure indicates a signi®cant difference between patient and controls. unknown people who had not been seen before (new lures). Stimuli were presented in random order without time constraint. Results J. R. and normal controls made correct fame judgements for 55 and 63% of faces with real, though modest celebrity, respectively (Table 8). For new lures (i.e. faces that had never been seen before), J. R. made false fame judgements as often as the controls (15 and 11%, respectively). Critically, when confronted with the old lures (i.e. unknown faces that had already been seen in a prior experiment), both J. R. and normal controls made more false fame judgements compared with the new lure faces [control mean: 32 versus 11%, c2(1) = 15.6, P = 0.0001; patient mean 80 versus 15%, P = 0.0001, Fisher's test] (Table 6). However, this increase in false fame judgements for old lures was much higher in J. R. than in normal subjects [c2(1) = 14.9, P = 0.0001], whereas her ability to reject new lure faces and to recognize real famous faces did not differ from that of normal subjects [c2(1) = 0.03 and 0.21, respectively]. These data reveal that J. R. was severely impaired in attributing a correct source to false signals of familiarity with unknown faces, and showed a marked bias towards considering unknown faces as known by fame based on coarse signals of subjective familiarity. False fame and prior name exposure To determine whether our patient's abnormal increase in false familiarity judgements was speci®c to faces or re¯ected a more general bias in assessing the source of subjective familiarity, a second task using names was given to her and the same controls in a different session. As in the previous face task, 60 proper names (e.g. Paul Martin) were presented singly and had to be judged as famous or unknown. The names included those of 20 people with real but modest fame Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Unknown people Famous people Real Outer contour chimaeras Inner eyes chimaeras Inner mouth chimaeras Relatives Real Outer contour chimaeras Inner eyes chimaeras Inner mouth chimaeras Mean reaction time (correct) 899 900 P. Vuilleumier et al. (e.g. minor politicians or artists), 20 unknown people already seen as distractors in a previous test (old lures), and 20 unknown people never seen before (new lures). Stimuli were presented in random order without time constraint. Results Associative processing and priming In the prior exposure experiments, our patient showed an abnormally high rate of familiarity misattribution for faces that were unknown but previously seen in a different context (but no such errors for names). This result reveals a marked bias towards considering unknown faces as famous when coarse signals of familiarity were elicited but failed to activate more speci®c information in memory (e.g. to identify the source of familiarity). This led us to consider whether J. R. had a particular de®cit in activating stored representations that give access to identity-speci®c knowledge about a face. This was examined in two different tests of face priming, as used previously in normal subjects (Bruce et al., 1993; Young et al., 1994) and prosopagnosics (De Haan et al., 1992): (i) visual repetition priming, which refers to facilitated recognition of a face that has been seen previously and re¯ects activation of the visual representation of this face (Bruce et al., 1993), possibly involving the right hemisphere (GruÈsser and Landis, 1991); and (ii) associative semantic priming, which involves facilitation of recognition based on some information linked to a given person (such as the name of the person or someone related), re¯ecting an activation of speci®c identity knowledge, is maximal when the prime and target concern the same individual (Young et al., 1994), and possibly implicating more the left hemisphere (Rhodes, 1985). Each test was given in a separate session. For visual priming (face±face task), a face was ®rst shown for 2 s (to be name aloud), and was immediately replaced by a second face (target) that remained on the screen until a familiarity decision (known/unknown) was made as quickly as possible on the latter by pressing one of two keys (Fig. 3A). For associative priming (name±face task), a name was ®rst shown for 2 s (to be read aloud), again it was replaced by a face (target) that remained on the screen until a speeded familiarity decision (Fig. 3B). Thus, in both tasks, familiarity Results Error rates were low in J. R. (4%) and healthy controls (8%) in both tasks. Median correct reaction times (RTs) were computed for each subject in each condition. Overall RTs were similar in J. R. (mean 691 ms) and controls (mean 677 ms) in each task (unpaired t test, P > 0.45). Priming effects were assessed by repeated-measures ANOVA (analysis of variance) on correct RTs to known faces, with the different prime types as a factor, ®rst across and then within individual controls to allow comparison with the patient. In the face±face task, healthy controls showed reliable visual priming (Table 9). There was a signi®cant effect of the preceding face type on RTs [F(3,5) = 3.79, P = 0.03], due to faster responses in the same-person condition compared with others [t(5) > 2.94, P < 0.05]. There was no signi®cant effect of same-category faces. J. R. showed the same pattern of signi®cant priming effects (Table 8) (F = 2.34, P = 0.045 in two different sessions), with faster responses after sameperson faces than after other face types (P < 0.05). The same results were obtained in a second session 2 weeks later, in which faces from close relatives (family and friends) were added to those of celebrities, using the same four priming conditions for the relatives and famous people as above (Table 8). Healthy subjects from the same family showed similar performance for both relatives and celebrities. These results demonstrate intact visual identity-priming in J. R. (Bruce et al., 1993). In the name±face task, healthy controls again showed signi®cant priming effects (Table 9) [F(3,7) = 7.36, P = 0.002]. Their RTs were faster after same-person names than in other conditions [t(7) > 3.1, P < 0.02], consistent with facilitation of face recognition by the activation of identity-speci®c associations (Young et al., 1994). There was no signi®cant effect of same-category names. These effects were found in each individual Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 J. R. correctly recognized real fame and correctly rejected new lures and controls did also (Table 8). Again, a signi®cant increase in false fame judgements occurred for old lures (i.e. previously exposed unknown names) compared with new lures, both in normal controls [mean 27 versus 8%, c2(1) = 14.7, P = 0.0001] and in the patient (30 versus 5%, P = 0.050, Fisher's test). However, the rate of such errors was not different between J. R. and controls [c2(1) = 0.06, P = 0.80]. This indicates that the patient's de®cit in associating subjective familiarity with a correct source was not present with names, but concerned faces selectively. decisions were always made on a face, but the face was preceded either by another face (face±face visual priming) or a written name (name±face semantic priming). Faces (and names) of 30 celebrities from three categories (politicians, actors, musicians) were selected to create 15 pairs of associated people, while 30 unknown faces (and 30 unknown names) served as unfamiliar stimuli. In each task, a famous face could be preceded by four possible primes (30 trials per condition): (i) the same person (but different pictures in the face±face task to prevent same-stimulus repetition); (ii) a related celebrity from the same category; (iii) a celebrity from another category; or (iv) a neutral unknown person. Unknown faces were also presented as ®llers, preceded by either a known celebrity or an unknown person (30 trials per condition). All trial types occurred in random order. The critical conditions concerned the effect of identity-speci®c priming for known faces, i.e. familiarity decisions that were made on a known face preceded by either the face or the name of the same person. Hyperfamiliarity for unknown faces 901 control. By contrast, J. R. showed a very abnormal pattern (Table 8). Whereas different name types had an effect in the ®rst session (F = 2.72, P = 0.022) but not in the second session (F = 1.23, P = 0.28), in both instances the same-person names tended to slow rather than facilitate familiarity decisions compared with neutral, unknown names (P < 0.05). Impaired identity-priming was replicated in both sessions for celebrities, and was similar for faces of relatives and celebrities in the second session (Table 8). Altogether, these priming results suggest a disturbance in activating identity-speci®c semantic associations in the patient when she made judgements of familiarity, despite normal activation of the visual representation of known faces (Bruce et al., 1993). Discussion We describe a young woman who, subsequent to a left temporal venous infarction, exhibited a disturbing feeling of familiarity, even intimacy, towards faces of people unknown to her. Although she had no dif®culty recognizing people who were already known, she mistook many new faces as belonging to people with whom she was well acquainted. Later, this phenomenon partly abated but remained more frequent in familiar surroundings, even 1 year after onset. In many respects, this disorder presented as the reverse of prosopagnosia. Whereas prosopagnosics typically have right inferior temporal lesions and no longer recognize familiar faces (Landis et al., 1986, 1988; De Renzi et al., 1994), our patient suffered left lateral temporal damage and experienced exaggerated familiarity with unknown faces, even though she could still identify known faces and learn new ones. Occasional feelings of false familiarity with unknown faces are not uncommon in normal people, though they are usually faint and are rapidly acknowledged as a trivial error (Young et al., 1985a). These impressions rarely lead to the conviction of intimately knowing a stranger, to the point of searching at length for any possible links, as in our patient. As an acute Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Fig. 3 Example of stimuli used to test face recognition priming. (A) Visual repetition priming (face±face task). On each trial, a target face was preceded by the face of the same or another person. (B) Associative semantic priming (name±face task). On each trial, a target face was preceded by the name corresponding to the same or another person. In both tasks, the subject had to make a speeded familiarity judgement (known/unknown) on the target face. 902 P. Vuilleumier et al. Table 9 Visual and semantic priming of face recognition Type of prime condition Face±face task (visual priming) Name±face task (semantic priming) Patient J. R. Controls* Patient J. R. Controls* 605 672 673 754 624 6 111 744 6 193 751 6 200 689 6 188 817 798 662 704 576 6 39 683 6 71 646 6 75 679 6 100 634 708 801 860 468 6 91 610 6 88 684 6 82 702 6 99 741 619 717 595 454 6 45 600 6 64 669 6 75 561 6 138 676 788 721 787 425 6 29 526 6 55 585 6 36 592 6 66 654 607 751 656 435 6 72 484 6 29 559 6 56 553 6 109 *Mean 6 SD of median reaction time. Controls were six age- and education-matched normal subjects (®ve females and one male, mean age 26.2 6 4.0 years) in the face±face task of session 1; eight matched normal subjects (six females and two males, mean age 26.3 6 4.5 years) in the name±face task of session 1; and four normal subjects of the same family (two females and two males, mean age 31.7 6 4.6 years) in both tasks of session 2. Signi®cant de®cits between the patient and controls are indicated in bold. neuropsychological impairment, in direct relation to a focal cortical lesion, this phenomenon has never been reported previously. Using standardized and ad hoc tests, we tried to clarify the nature of this disorder. Tests designed to uncover various forms of prosopagnosia showed that our patient's face recognition abilities were in the upper part of the range of normal subjects. The same was true for memory, basic visual perception and a comprehensive neuropsychological examination. Thus, J. R. was clearly not prosopagnosic and her false familiarity could not be explained by a basic recognition de®cit or general cognitive disturbances. Furthermore, her errors did not involve the misidenti®cation of speci®c individuals and delusional elaboration, as in FreÂgoli syndrome (Ellis and Young, 1990). False face recognition has rarely been observed without prosopagnosia in patients with right brain damage and piecemeal visual processing, in whom misidenti®cation may result from resemblance to the local facial features of a known person (Young et al., 1993; Rapcsak et al., 1994). Misidenti®cation can also occur without visual de®cit in patients with frontal damage and confabulation, due to impaired monitoring (Rapcsak et al., 1998, 1999) or inappropriate semantic associations (Ward et al., 1999). These conditions all differ clearly from those of our case. J. R. showed no frontal dysfunction, confabulation or delusion. She performed normally on a variety of discrimination, identi®cation and memory tasks with faces and showed normal visual-repetition priming for known faces, suggesting preserved perceptual input and preserved formation of structural facial representations. Among the variety of tests tapping different levels of face processing, three signi®cant de®cits were found in J. R.: (i) de®cient use of internal face parts to guide recognition; (ii) lack of face-identity priming by known names during familiarity judgements; and (iii) abnormal misattribution of fame to unknown faces after incidental prior exposure. We suggest that all three de®cits may similarly point to a deterioration of face processing involving the left hemisphere and greater reliance on right hemisphere function. First, J. R. showed dif®culty recognizing upside-down faces (inverted face task), with a tendency to rely more on external and global features and less on internal parts (altered face task) compared with normal subjects. It is known that inversion suppresses the right-hemispheric advantage for face recognition and requires the greater featural analysis mediated by the left hemisphere (e.g. Hillger and Koenig, 1991). Moreover, although J. R. exhibited normal discrimination sensitivity (d¢) for recognizing isolated features (face part task), her response criterion (i.e. her subjective certainty) appeared looser than that of normal subjects. Overall, this would be consistent with relative failure to encode internal facial parts by visual processes that depend on the left hemisphere, and greater reliance on right-hemisphere processes encoding global features instead (Tanaka and Farah, 1993). Since internal features are more important for identifying known faces (Ellis et al., 1979; Young et al., Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 Session 1: faces of celebrities Same person Related person Unrelated person Unknown person Session 2: faces of celebrities and relatives Celebrities Same person Related person Unrelated person Unknown person Relatives Same person Related person Unrelated person Unknown person Median reaction time (ms) Hyperfamiliarity for unknown faces face was elicited almost three times more often in J. R. than in normal subjects. Such a de®cit was not found with names, demonstrating that it was speci®c to faces. Since other tests revealed that J. R. was unimpaired in judging whether a face had already been presented (e.g. in memory tasks), it must be concluded that her problem arose at the stage where a personal association is evoked by seen faces, leading to a subjective meaning, such as fame or personal acquaintance (Damasio et al., 1990). This pathological rate of false fame judgements in J. R. suggests an exaggerated bias towards attributing personal meaning to unknown faces in the presence of only minimal signals of familiarity (such as those induced by incidental prior exposure in this task). This misattribution of familiarity was speci®c to faces and unlikely to re¯ect more general problems of memory source attribution, confabulation or dysexecutive impairment, given her good performance in other general neuropsychological tests. Semantic memory also appeared intact, including knowledge about people (e.g. the Dead±Alive test) and naming, although more formal testing of semantic memory was not conducted. In normal subjects, a misattribution of subjective familiarity can also be induced by spurious signals based on unconscious inferences and expectations, when more precise information about the source of familiarity cannot be accessed (Bartlett et al., 1991; Whittlesea and Williams, 1998; Yonelinas et al., 1999). Impaired access to personspeci®c associations was evidenced in J. R. by her lack of identity priming in the name±face task, indicating that she judged face familiarity without accessing semantic representations pertaining to identity-speci®c knowledge (such as names), unlike normal subjects (Young et al., 1994). The fact that she was much more prone to falsely recognizing fame in unknown faces, even without accessing more precise information in memory, indicates that unconscious signals of familiarity induced by the non-remembered prior exposure with these faces was suf®cient to produce a much stronger feeling of knowing these faces in her than in normal subjects (Whittlesea and Williams, 1998). These ®ndings therefore suggest not only decreased activation of speci®c semantic associations about seen faces, but also a greater tendency to activate associations of personal and affective meaning (Van Lancker, 1991). This would be compatible with an imbalance of face recognition mechanisms caused by impaired processing in the left hemisphere and the release of right hemisphere processes, in the context of interactive callosal inhibition between hemispheric functions (Regard et al., 1994; Cook et al., 1995). Broad and unconsciously generated associations about people might be more readily activated in the right hemisphere, even by occasional unknown faces, and underlie a subjective feeling of personal relevance and affective relationship (Van Lancker, 1991; Seeck et al., 1993), while the concomitant activation of more precise associations in the left hemisphere would be necessary in order to focus recognition on speci®c semantic knowledge related to a single individual (Rhodes, 1985; Damasio et al., 1990; Verstichel, 2001). Downloaded from https://academic.oup.com/brain/article/126/4/889/331955 by guest on 11 April 2024 1985b), erroneous familiarity might have arisen from resemblance to known faces on the basis of global or external traits, in contrast to the piecemeal visual errors of right braindamaged patients (Rapcsak et al., 1994). However, de®cient processing of internal facial parts with false familiarity based on global traits is not suf®cient to explain J. R.'s disorder because she made no false recognitions of chimaeric faces that contained familiar external features with unknown internal parts, and she could easily recognize caricatures in which distinctive features were exaggerated and con®gurational cues were distorted (Rhodes et al., 1987). Therefore, whereas an abnormal bias towards basing recognition on global facial traits processed in the right hemisphere could expose J. R. to spurious familiarity signals, some additional factor must be necessary for such signals to be accepted subjectively by the patient as compelling feelings of personally knowing a face. Note that, in all of the above tests assessing the recognition of altered faces or features, judgements of familiarity required a decision as to whether a facial stimulus had already been seen or not, and in such tests J. R. showed excellent discrimination and memory abilities. However, her abnormal feeling of familiarity with strangers in real life involved more than a false judgement of past occurrence: she had a compelling sentiment of knowing a person, with a strong feeling of personal closeness and intimacy. The subjective recollective experience triggered by seeing an individual face is inherently dependent on the activation of a complex network of associations between the visual representation of that face and other stored knowledge, such as speci®c biographical details, relevant episodes, particular contextual situations, and affective links (Rhodes, 1985; Damasio et al., 1990). A disorder within this network in our patient might have altered the pattern of associations evoked by unknown faces and distorted her subjective experience of familiarity. In line with this, two other signi®cant de®cits in J. R. were observed in tests that required a face to be associated with distinctive information in memory, unique to the identity of a known or previously seen person. Thus, she showed a selective loss of identity-speci®c facilitation in the name±face priming task (despite intact visual priming in the face±face task), and a highly pathological rate of false fame attributions to unknown faces after incidental prior exposure. Both de®cits suggest a problem in the associative processes involved in the recognition of a person (Burton et al., 1990; Young et al., 1994), at the level where speci®c knowledge pertaining to identity (e.g. a proper name in the semantic priming task, or a unique contextual trace in the false fame task) must be accessed from visual facial cues. In fact, the most striking de®cit of J. R. in experimental tests of familiarity was observed in the false fame task, in which she had to judge not whether a face had been seen before, but whether it was known by fame. In this task, she mistook as famous ~80% of the faces that were basically not known but had been seen just once before in earlier experiments. This false feeling of having personal knowledge about an unknown 903 904 P. Vuilleumier et al. semantically related faces (Damasio et al., 1988), which is consistent with a role of the left temporal cortex in retrieving information about known people. However, the contribution of perceptual or naming dif®culties may be dif®cult to establish in such cases because of the larger extent of cortical and subcortical damage caused by arterial occlusion. In summary, this case extends other reports suggesting that abnormal face familiarity can arise from de®cits at several stages of processing (Young et al., 1993; Rapcsak et al., 1999; Ward et al., 1999). This implicates the activation of associative networks integrating facial cues with more complex representations of personal relevance (Burton et al., 1990; Damasio et al., 1990; Schreiber et al., 1991; Hanley et al., 1998) rather than only the abnormal activation of the visual representation of known faces, as proposed by earlier models (Bruce and Young, 1986). To our knowledge, this case constitutes a new neuropsychological disorder that demonstrates that both hemispheres have a signi®cant role in face processing. Acknowledgements We wish to thank colleagues and students who participated in the experiments as control subjects, Tim Shallice, Bob Rafal, Jamie Ward, Sophie Schwartz and Frederic Assal for helpful comments and support, Margitta Seeck for providing face stimuli, Claire Bindschaedler for providing tests and norms, and the patient and her family for their cooperation. This work was partly supported by grants from the Swiss National Science Foundation to P.V. 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R. in the chronic stage occurred in familiar places (e.g. university) in which many seen faces had no identity-speci®c representation other than a link with this familiar context (Davies, 1988). In such conditions, contextual cues can in¯uence the perceived familiarity of faces (Young et al., 1985a; Davies, 1988). Greater reliance on right-hemisphere associative networks in J. R. might therefore facilitate the misattribution of personal meaning to unknown faces (as shown experimentally in the false fame task), especially in the presence of spurious signals of familiarity evoked by non-speci®c cues (Thompson et al., 1982; Tiberghien, 1986; Bartlett et al., 1991; Whittlesea and Williams, 1998). An imbalance between reciprocal hemispheric functions to account for J. 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Our normal subjective experience of knowing a seen face may depend critically on coordinated activity within this bilateral network, linking the visual representation of faces and other contextual cues to stored associations pertaining to person identity and affective relevance (Damasio et al., 1990; Van Lancker, 1991). While face recognition disorders are rare after left brain damage (Warrington and James, 1967), J. R. had a very unusual lesion due to cortical venous thrombosis, centred on the posterior middle temporal gyrus. Such venous lesions may affect different brain regions and cause only partial cortical damage rather than complete destruction of brain tissue, as do arterial infarcts. Moreover, episodes of false familiarity may be missed if the patient does not complain spontaneously or has larger lesions, resulting in aphasic and naming disorders. 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