Leukoencephalopathy, diffuse hereditary, with spheroids 1

MONDO:0800027

A rare autosomal dominant disease characterized by a complex phenotype including progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy.

Also known as: HDLS, hereditary diffuse leukoencephalopathy with spheroids, leukoencephalopathy, diffuse hereditary, with spheroids, leukoencephalopathy, hereditary diffuse, with spheroids, ALSP, Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia, CSF1R-related ALSP, CSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

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

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