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.
Read more about Leukoencephalopathy With Vanishing White Matter: Synonyms, History, Causes/Description, Symptoms, Neuropathology, Diagnosis, Epidemiology, Treatment
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