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adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

ORPHA: 313808

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

leukodystrophy that is characterized by progressive dementia, apraxia, apathy, impaired balance, parkinsonism, spasticity and epilepsy and has material basis in heterozygous mutation in the CSF1R gene on chromosome 5q32

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

Orphanet Code

ORPHA:313808
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
OrphanetORPHA:313808
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | OrphanDrug