Also Known As
HDLShereditary diffuse leukoencephalopathy with spheroidsleukoencephalopathy, diffuse hereditary, with spheroidsleukoencephalopathy, hereditary diffuse, with spheroidsALSPAdult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented GliaCSF1R-related ALSPCSF1R-related adult-onset leukoencephalopathy with axonal spheroids and pigmented gliaFPSGGPSCPOLDadult-onset leukoencephalopathy with axonal spheroids and pigmented gliaautosomal dominant leukoencephalopathy with neuroaxonal spheroidsdementia, familial, Neumann typefamilial dementia, Neumann typefamilial progressive subcortical gliosisgliosis, familial progressive subcorticalleukoencephalopathy with neuroaxonal spheroids, autosomal dominantleukoencephalopathy, adult-onset, with axonal spheroids and pigmented gliapigmentary orthochromatic leukodystrophysubcortical gliosis of Neumannadult-onset leukodystrophy with neuroaxonal spheroidshereditary diffuse leukoencephalopathy with axonal spheroidsneuroaxonal leukodystrophy
Definition
A rare autosomal dominant disease characterized by a complex phenotype including progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy.