Gerstmann-Straussler-Scheinker disease : KMLE 의학 검색 엔진 - 의학사전, 의학용어, 의학약어, 의학논문, 약품/의약품 검색

MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 1 페이지: 1

Gerstmann-Straussler-Scheinker Disease - 새창 An autosomal dominant familial prion disease with a wide spectrum of clinical presentations including ATAXIA, spastic paraparesis, extrapyramidal signs, and DEMENTIA. Clinical onset is in the third to sixth decade of life and the mean duration of illness prior to death is five years. Several kindreds with variable clinical and pathologic features have been described. Pathologic features include cerebral prion protein amyloidosis, and spongiform or neurofibrillary degeneration. (From Brain Pathol 1998 Jul;8(3):499-513; Brain Pathol 1995 Jan;5(1):61-75)
Synonyms : Gerstmann-Straussler Inherited Spongiform Encephalopathy, Inherited Spongiform Encephalopathy, Gerstmann-Straussler, Gerstmann Straussler Inherited Spongiform Encephalopathy, Gerstmann Straussler Scheinker Disease, Gerstmann Straussler Syndrome