| GSD | genetically significant dose; Gerstmann-Straussler disease; glutathione synthetase deficiency; glyco... |
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| GSS | gamete-shedding substance; General Social Survey; Gerstmann-Straussler-Scheinker [disease] |
| GSSD | Gerstmann-Straussler-Scheinker disease |
| GSS | Gerstmann-Straussler-Scheinker Syndrome |
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| GSS | Gerstmann-Straussler-Scheinker |
| GSS | Gerstmann-Straussler-Scheinker disease |
| Straussler | See: Gerstmann-Straussler-Scheinker syndrome. (05 Mar 2000) |
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| Gerstmann-Straussler-Scheinker syndrome | <syndrome> A familial spongiform encephalopathy. Transgenic mice with a mutant form of the PrP gene from patients with this syndrome develop degenerative brain disease that is similar, but not identical, to that caused by scrapie. It is a more chronic cerebellar form of spongiform encephalopathy, producing a neurodegenerative condition that has morphological similarities to Creutzfeldt-Jakob syndrome. However, in this syndrome there is slower progression, signs of spinocerebellar ataxia, and the spongiosis is less pronounced. Prion proteins and amyloid plaques are found in the brain of patients with the syndrome. A germline mutation of the prion protein has been demonstrated. (12 Jul 2000) |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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