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  • Adult-onset leukoencephalopathy with axonal spheroids and pigmented . . .
    Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a neurological condition characterized by changes to certain areas of the brain A hallmark of ALSP is leukoencephalopathy, which is the alteration of a type of brain tissue called white matter
  • About ALSP - ALSP Info
    Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a fatal, rare, hereditary, and rapidly progressive neurodegenerative disease 1,2 ALSP is a primary microgliopathy5
  • Sisters Hope Foundation ALSP
    Patient advocacy group for those diagnosed with ALSP, adult-onset leukoencephalopathy with axonal spheroids and pigmented glia, HDLS and CSF1R related disorders Support, information and resources for leukodystrophy and ALSP patients and caregivers
  • Adult-onset diffuse leukoencephalopathy with axonal spheroids and . . .
    Adult-onset diffuse leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a rare progressive degenerative white matter disease caused by mutations in the colony-stimulating factor-1 receptor gene
  • Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented . . .
    Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a term that refers to the characteristic brain tissue findings in affected people People with ALSP present with a rare and progressive neurological disease in which the brain tissue known as white matter wastes away (leukodystrophy) forming lesions in certain
  • ALSP Symptoms and Causes - Sisters Hope Foundation
    Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a rare, progressive neurological condition characterized by changes to the white matter of the brain
  • ALSP Info
    ALSP is an acronym for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia It is a rare genetic disease caused by a defect in the DNA, or mutation, of the CSF1R gene
  • Adult-onset leukoencephalopathy with axonal spheroids and pigmented . . .
    Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP), also known as hereditary diffuse leukoencephalopathy with spheroids (HDLS) and pigmentary orthochromatic leukodystrophy (POLD), refers to a rare inherited autosomal dominant disease characterized by an adult-onset leukodystrophy that usually leads to death in
  • Adult-onset leukoencephalopathy with axonal spheroids and . . . - MedlinePlus
    Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a neurological condition characterized by changes to certain areas of the brain A hallmark of ALSP is leukoencephalopathy, which is the alteration of a type of brain tissue called white matter





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