Conditions / Genetic

leukoencephalopathy with vanishing white matter

info · Genetic · ICD-10: E75.2

A leukodystrophy characterized by variable neurologic features resulting from deficiency in astrocyte maturation, including progressive cerebellar ataxia, spasticity, and cognitive impairment associated with white matter lesions on brain imaging with onset fro

A leukodystrophy characterized by variable neurologic features resulting from deficiency in astrocyte maturation, including progressive cerebellar ataxia, spasticity, and cognitive impairment associated with white matter lesions on brain imaging with onset from early infancy to adulthood.

Also known as: CACH; CACH/VWM; childhood ataxia with central nervous system hypomyelination; vanishing white matter leukodystrophy