hypomyelination

hypomyelination
hy·po·my·e·lin·a·tion (hi″po-mi″ə-lin-aґshən) disappearance, or inadequate formation, of myelin sheaths on nerves.

Medical dictionary. 2011.

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  • hypomyelination — noun An abnormally small amount of myelin in the brain and spinal cord Syn: dysmyelination …   Wiktionary

  • hypomyelination, hypomyelinogenesis — Defective formation of myelin in the spinal cord and brain; the basis for a number of demyelinating diseases …   Medical dictionary

  • childhood ataxia with central nervous system hypomyelination — vanishing white matter disease …   Medical dictionary

  • 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

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  • 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

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  • Zellweger syndrome — Classification and external resources ICD 10 Q87.8 ICD 9 277.86 …   Wikipedia

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