4 patients with prosopagnosia are described. They presented associated neuropsychological deficits (achromatopsia, topographical disorientation) and visual field defects. In 1 case, gross pathological examination revealed bilateral symmetrical infero-medial occipito-temporal infarcts. In 2 other cases, computer tomography (CT) demonstrated bilateral inferior temporo-occipital infarction. In 1 case CT showed only occipital infarctions in the occipital lobes. This brings to 16 the number of anatomically studied cases of prosopagnosia (8 by necropsy, 8 by CT). In contrast to clinical localization, which often indicates only a right cerebral lesion, all anatomically verified cases of prosopagnosia exhibit bilateral lesions in the posterior cerebral artery distribution.
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http://dx.doi.org/10.1159/000115494 | DOI Listing |
Cortex
November 2024
Department of Psychology, Bournemouth University, Faculty of Science and Technology, Poole House, Fern Barrow, Poole, UK.
Poor performance on cognitive assessment tasks may indicate a selective 'impairment'. However, it is unclear whether such difficulties separate the individual from the general population qualitatively (i.e.
View Article and Find Full Text PDFEpilepsy Behav Rep
August 2024
Department of Neurology, University of Wisconsin-Madison, USA.
Prosopagnosia, a neurological condition affecting perception and differentiation of faces, is categorized as either acquired or developmental (present since birth). Acquired cases of prosopagnosia are usually caused by right hemisphere or bilateral damage. We present a right-handed 17-year-old male with a history of focal epilepsy and a new diagnosis of prosopagnosia due to a perinatal stroke affecting the left lingual gyrus, a structure in close proximity to the fusiform face area.
View Article and Find Full Text PDFBehav Res Methods
October 2024
Department of Psychology, Swansea University, Swansea, UK.
The Diagnostic Statistical Manual of Mental Disorders (DSM-5) recommends diagnosing neurocognitive disorders (i.e., cognitive impairment) when a patient scores beyond - 1 SD below neurotypical norms on two tests.
View Article and Find Full Text PDFNeuropsychologia
June 2024
Centre for Biomedical Technologies, Queensland University of Technology, Australia; Université de Lorraine, CNRS, IMoPA, F-54000, Nancy, France. Electronic address:
Facial identity recognition (FIR) is arguably the ultimate form of recognition for the adult human brain. Even if the term prosopagnosia is reserved for exceptionally rare brain-damaged cases with a category-specific abrupt loss of FIR at adulthood, subjective and objective impairments or difficulties of FIR are common in the neuropsychological population. Here we provide a critical overview of the evaluation of FIR both for clinicians and researchers in neuropsychology.
View Article and Find Full Text PDFBrain Commun
January 2024
Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA.
Loss of facial recognition or prosopagnosia has been well-recognized for over a century. It has been categorized as developmental or acquired depending on whether the onset is in early childhood or beyond, and acquired cases can have degenerative or non-degenerative aetiologies. Prosopagnosia has been linked to involvement of the fusiform gyri, mainly in the right hemisphere.
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