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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 translation initiation factor EIF-2B: EIF2B1, EIF2B2, EIF2B3, EIF2B4, or EIF2B5. The disease belongs to a family of conditions called the Leukodystrophies. == Synonyms == * childhood ataxia with central nervous system hypomyelinization; CACH * vanishing white matter leukodystrophy *Cree leukoencephalopathy; CLE * vanishing white matter leukodystrophy with ovarian failure, included * ovarioleukodystrophy, included * myelinopathia centralis diffusa 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「leukoencephalopathy with vanishing white matter」の詳細全文を読む スポンサード リンク
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