Leukoencephalopathy with vanishing white matter 1

MONDO:0020507

Any leukoencephalopathy with vanishing white matter in which the cause of the disease is a variation in the EIF2B1 gene.

Also known as: CACH, childhood ataxia with central nervous system hypomyelinization, vanishing white matter leukodystrophy, Cree leukoencephalopathy

19 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by