(VWM disease) is an
Autosomal Recessive neurological disease. The cause of the disease are mutations in any of the 5
Gene s encoding subunits of the
Translation Initiation Factor EIF2B : EIF2B1, EIF2B2, EIF2B3, EIF2B4, or EIF2B5.
Adult-onset VWM disease can present with
Psychosis and may be hard to differentiate from
Schizophrenia .
1
- 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
