- childhood ataxia with central nervous system hypomyelination
- vanishing white matter disease.
Medical dictionary. 2011.
Medical dictionary. 2011.
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