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Up to: Leukodystrophy · Leukoencephalopathy, hereditary diffuse, with spheroids · CSF1R-related disorder
Leukoencephalopathy, diffuse hereditary, with spheroids 1
A rare autosomal dominant disease characterized by a complex phenotype including progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy.
This condition has no sub-types.