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leukoencephalopathy, progressive, with ovarian failure

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive neurodegenerative disorder characterized by childhood- to adulthood-onset of signs of neurologic deterioration consisting of ataxia, spasticity, and cognitive decline with features of frontal lobe dysfunction. Brain MRI shows leukoencephalopathy with striking involvement of deep white matter, and cerebellar atrophy. All female patients develop premature ovarian failure.
Mondo Term and Equivalent IDs
MONDO:0014387:  leukoencephalopathy, progressive, with ovarian failure
UMLS:C4014588: