childhood ataxia with central nervous system hypomyelination

childhood ataxia with central nervous system hypomyelination
vanishing white matter disease.

Medical dictionary. 2011.

Игры ⚽ Нужен реферат?

Look at other dictionaries:

  • Leukoencephalopathy with vanishing white matter — Classification and external resources OMIM 603896 Leukoencephalopathy with vanishing white matter (VWM disease) is an autosomal recessive neurological disease. The cause of the disease are mutations in any of the 5 genes encoding subunits of the… …   Wikipedia

  • EIF2B2 — Eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa, also known as EIF2B2, is a human gene.cite web | title = Entrez Gene: EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa| url =… …   Wikipedia

  • EIF2B1 — Eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa, also known as EIF2B1, is a human gene.cite web | title = Entrez Gene: EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa| url =… …   Wikipedia

  • Syndrome CACH — Référence MIM 603896 Transmission Récessive Chromosome 1p34.1 2p23.3 2p23.3 12 14q24 Gène EIF2B …   Wikipédia en Français

  • vanishing white matter disease — an autosomal recessive type of leukodystrophy, seen most often in young children, characterized by hypomyelination of variable severity; it usually develops slowly, although there may be rapid deterioration after an infection or head trauma.… …   Medical dictionary

  • List of diseases (C) — A list of diseases in the English wikipedia.C* C syndrome * C1 esterase deficiency (angioedema)CaCac Cal* Cacchi Ricci disease * CACH syndrome * Cafe au lait spots syndrome * Caffey disease * CAHMR syndrome * Calcinosis cutis (see also CREST… …   Wikipedia

Share the article and excerpts

Direct link
Do a right-click on the link above
and select “Copy Link”