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Prosopagnosia: a rare presenting manifestation of frontotemporal lobar degeneration.

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Frontotemporal dementia is an important neurodegenerative disorder accounting for a significant proportion of dementia cases with onset before 60 years of age. Apart from the well recognized behavioral changes the disease has many other distinctive features like predominant language involvement

Progressive prosopagnosia associated with selective right temporal lobe atrophy. A new syndrome?

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V.H., a 68-year-old right-handed woman, presented with a progressive deterioration in her ability to recognize faces of familiar people, including friends and relatives. Neuropsychological testing on two occasions separated by 9 months indicated no deterioration in general intellectual ability from

Impaired configurational processing in a case of progressive prosopagnosia associated with predominant right temporal lobe atrophy.

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F.G., a 71-year-old right-handed man, presented with a slowly progressive deterioration in his ability to recognize faces of familiar and famous persons, contrasting with the relative preservation of other cognitive domains. His primary face perception skills were intact. Along with his

[Progressive prosopagnosia associated with selective right temporal lobe atrophy].

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[Progressive prosopagnosia associated with right temporal atrophy in a patient with hereditary dementia].

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[Confirmation of cortical lesions of progressive prosopagnosia by cerebral SPECT].

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We present the case of a 78 year old man admitted to the hospital with progressive memory disorder. Neuropsychological examination showed inability to recognize familiar faces (prosopagnosia). MRI documented cortical atrophy, which did not explain the neurological deficit. CT did not show

Progressive ventral posterior cortical degeneration presenting as alexia for music and words.

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Patients with posterior cortical atrophy may have dorsal visual system (occipital-parietal) dysfunction (optic ataxia, visuospatial disorientation, and simultanagnosia), ventral visual system (occipital-temporal) dysfunction (pure alexia, prosopagnosia, visual anomia, and agnosia), or both. We

Complex visual hallucination and mirror sign in posterior cortical atrophy.

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OBJECTIVE In posterior cortical atrophy (PCA), visual hallucinations are rare symptoms and mirror sign has not been described. METHODS Single case report. RESULTS We reported a 60-year-old woman with PCA who reported complex visual hallucinations, such as a man walking in her room, and mirror sign,

A novel PSEN1 (S230N) mutation causing early-onset Alzheimer's Disease associated with prosopagnosia, hoarding, and Parkinsonism.

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We describe clinical and biomarker findings in an index patient with the onset of Alzheimer's disease (AD) symptoms at age 57 and a family history consistent with an autosomal dominant pattern of inheritance. She had the atypical early features of visual agnosia and prosopagnosia followed by

[Homonymous hemianopia and posterior cortical atrophy].

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BACKGROUND Posterior cortical atrophy (PCA) is a clinically and radiologically defined syndrome, in which predominant symptoms focus on higher visual dysfunction with progressive course and association with cortical atrophy or hypometabolism that predominates in the posterior part of the

[A case of cerebral vascular disease associated with prosopagnosia and minor hemisphere syndrome (author's transl)].

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A case of "apractognosia", a syndrome of minor hemisphere, and prosopagnosia was described. A 68 years old, right handed, hypertensive man who had experienced an episode of left hemiparesis of several weeks' duration developed a syndrome of minor hemisphere, metamorphopsia, visuoconstructive

Is this a new type of primary prosopagnosia, both progressive and apperceptive?

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Prosopagnosia, the inability to recognize faces, has a history going back to Charcot and Hughlings-Jackson, but was first named by Bodamer in 1947. Its anatomical loci are still unclear. However, progressive prosopagnosia is normally linked to right dominant temporal lobe atrophy, and diagnosed as

Covert person recognition: its fadeout in a case of temporal lobe degeneration.

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Covert person recognition was investigated longitudinally over a three-year period in a patient suffering from "Crossmodal Familiar Person Agnosia", possibly due to a fronto-temporal dementia in its right temporal variant (Gentileschi et al., 2001). The progressive neuronal degeneration in the

Right Temporal Lobe Atrophy: A Case That Initially Presented as Excessive Piety.

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OBJECTIVE Variants of frontotemporal lobar degeneration (FTLD) are associated with distinct clinical, pathological, and neuroanatomical profiles. Lines of emerging research indicate a rare variant with focal atrophy of the right temporal lobe (RTLA). The objective was to present case data and

[The clinical syndrome of posterior cortical atrophy].

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Posterior cortical atrophy (PCA) is a syndrome that involves distinct neuropsychological deficits. This paper presents the clinical and neuropsychological findings recorded in four patients with PCA and reviews the characteristics of the syndrome and other conditions that need to be considered in

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