| DGS | decompression sickness; developmental Gerstmann syndrome; diabetic glomerulosclerosis; Di George seq... |
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| GSD | genetically significant dose; Gerstmann-Straussler disease; glutathione synthetase deficiency; glyco... |
| 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-Strausler syndrome |
| GSS | Gerstmann-Straussler-Scheinker |
| GSS | Gerstmann-Straussler-Scheinker disease |
| Gerstmann syndrome | <syndrome> Tetrad of finger agnosia, dysgraphia or agraphia, dyscalculia or acalculia, and right-left disorientation producing confusion of laterality of the body. The syndrome can occur in brain-damaged and apparently normal children as well as in adults who have had vascular accidents, and is caused by lesions between the occipital area and the angular gyrus. (12 Jul 2000) |
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| Gerstmann, Josef | <person> Austrian neurologist, 1887-1969. See: Gerstmann syndrome, Gerstmann-Straussler-Scheinker syndrome. (05 Mar 2000) |
| 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) |
Synonyms : Acquired Gerstmann Syndrome, Acquired Gerstmann's Syndrome, Developmental Gerstmann's Syndrome, Gerstmann's Syndrome, Developmental Gerstmanns Syndrome, Finger-Agnosia-Left-Right-Confusion-Acalculia-Agraphias, Gerstmann Syndrome, Acquired, Syndrome, Gerstmann
Synonyms : Gerstmann-Straussler Inherited Spongiform Encephalopathy, Inherited Spongiform Encephalopathy, Gerstmann-Straussler, Gerstmann Straussler Inherited Spongiform Encephalopathy, Gerstmann Straussler Scheinker Disease, Gerstmann Straussler Syndrome
| Gerstmann syndrome |
The inability to recognize and use the fingers, differentiate left from right, problems writing and problems calculating, due to angular gyrus damage.
Ãâó: www.lieberson.com/en/neurgosurgery_glossary/g.htm
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| Gerstmann's s. |
a combination of finger agnosia, right-left disorientation, agraphia, acalculia, and often constructional apraxia; it was formerly attributed to a lesion in the angular gyrus of the dominant hemisphere, but now that etiology is in doubt.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Gerstmann's syndrome |
see under syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Gerstmann-Sträussler s. |
a group of rare prion diseases, of autosomal dominant inheritance but linked to different mutations of the prion protein gene, having the common characteristics of cognitive and motor disturbances and the presence of multicentric amyloid plaques in the brain. In the ataxic form, there are progressive cerebellar ataxia and dementia; in the telencephalic form, there are dysarthria, dementia, rigidity, tremor, and hyperreflexia; in GSS with neurofibrillary tangles, there are progressive short-term memory loss and clumsiness. Death occurs in 1 to 5 years.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| Gerstmann-Sträussler syndrome |
Gerstmann-Strässler-Scheinker syndrome.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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