Leukoencephalopathy with vanishing white matter information
Neurological disease
Medical condition
Leukoencephalopathy with vanishing white matter
Other names
Childhood ataxia with central nervous system hypomyelinization, Vanishing white matter leukodystrophy, Cree leukoencephalopathy, Vanishing white matter leukodystrophy with ovarian failure, included, Myelinopathia centralis diffusa
This condition is inherited in an autosomal recessive manner
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 eIF2B: EIF2B1, EIF2B2, EIF2B3, EIF2B4, or EIF2B5. The disease belongs to a family of conditions called the Leukodystrophies.[citation needed]
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Cerebrospinal Fluid Glycine: A Biochemical Marker for a LeukoencephalopathyWithVanishingWhiteMatter". Journal of Child Neurology. 14 (11): 728–731. doi:10...
subunits of translation initiation factor eIF2B can cause leukoencephalopathywithvanishingwhitematter". Ann. Neurol. 51 (2): 264–70. doi:10.1002/ana.10112...
subunits of translation initiation factor eIF2B can cause leukoencephalopathywithvanishingwhitematter". Ann. Neurol. 51 (2): 264–70. doi:10.1002/ana.10112...
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