DRPLA

DRPLA
Сокращение: Dentatorubral-pallidoluysian atrophy

Универсальный англо-русский словарь. . 2011.

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Смотреть что такое "DRPLA" в других словарях:

  • DRPLA — dentorubral pallidoluysian atrophy * * * dentatorubral pallidoluysian atrophy …   Medical dictionary

  • 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


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