NR AMBC

AU Vinters,H.V.; Hudson,A.J.; Kaufmann,J.C.E.

TI Gerstmann-Sträussler-Scheinker disease: autopsy study of a familial case.

QU Annals of Neurology 1986 Oct; 20(4): 540-3

PT journal article

AB Postmortem neuropathological findings in a patient with biopsy-proved familial Gerstmann-Sträussler-Scheinker disease of eight years' duration included severe spongy change in the neocortex, extensive and often large amyloid deposits throughout the cerebral hemispheres and cerebellum, and severe astrocytic gliosis throughout all areas of gray and white matter within the brain. The degree of cortical spongy change was much greater than that in relatives who died with a similar clinical history, indicating the phenotypic heterogeneity in this familial disorder.

MH Case Report; Central Nervous System/*pathology; Cerebellar Ataxia/*genetics/pathology; Dementia/*genetics/pathology; Female; Human; Middle Age; Reflex, Abnormal/*genetics/pathology; Support, Non-U.S. Gov't; Syndrome

SP englisch

PO USA

EA pdf-Datei

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