- DRPLA
- dentorubral-pallidoluysian atrophy
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dentatorubral-pallidoluysian atrophy.
Medical dictionary. 2011.
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dentatorubral-pallidoluysian atrophy.Medical dictionary. 2011.
DRPLA — • dentorubral pallidoluysian atrophy … Dictionary of medical acronyms & abbreviations
dentatorubral-pallidoluysian atrophy — (DRPLA) an autosomal dominant neurodegenerative syndrome of myoclonic epilepsy, dementia, ataxia, and choreoathetosis, with combined degeneration of the dentatorubral and pallidoluysian systems. Onset is usually in early adulthood, and it has… … Medical dictionary
Dentatorubral-pallidoluysian atrophy — Classification and external resources OMIM 125370 DiseasesDB 32909 MeSH … Wikipedia
ATN1 — is a protein found in nervous tissue.It is associated with a form of trinucleotide repeat disorder known as dentatorubral pallidoluysian atrophy or dentatorubropallidoluysian atrophy . PBB Summary section title = summary text = Dentatorubral… … Wikipedia
Trinucleotide repeat disorder — Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation … Wikipedia
Maladie De Naito-Oyanagi — Autre nom {{{Autre nom}}} Référence MIM … Wikipédia en Français
Maladie de Naito-Oyanagi — Référence MIM 125370 140340 Transmission Dominante Chromosome 12p13.3 Gène ATN1 … Wikipédia en Français
Maladie de naito-oyanagi — Autre nom {{{Autre nom}}} Référence MIM … Wikipédia en Français
Dementia — For other uses, see Dementia (disambiguation). Dementia Classification and external resources ICD 10 F00 F07 ICD 9 … Wikipedia
Spinocerebellar ataxia — (SCA) is a genetic disease with multiple types, each of which could be considered a disease in its own right. ymptomsSpinocerebellar ataxia (SCA) is one of a group of genetic disorders characterized by slowly progressive incoordination of gait… … Wikipedia