A Novel CSF1R Mutation in a Patient with Clinical and Neuroradiological Features of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids

J Alzheimers Dis. 2015;47(2):319-22. doi: 10.3233/JAD-150097.

Abstract

Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) is an autosomal dominant cerebral white matter degeneration leading to progressive cognitive and motor dysfunction. The peripheral nervous system is generally spared. Recently, mutations in the colony-stimulating factor-1 receptor (CSF1R) gene have been shown to be associated with HDLS. Here we report a new case of HDLS, carrying a mutation in CSF1R and manifesting rapidly progressive dementia and peripheral neuropathy.

Keywords: CSF1R; HDLS; leukoencephalopathy; presenile dementia.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Brain / pathology*
  • Brain / physiopathology
  • Humans
  • Leukoencephalopathies / genetics*
  • Leukoencephalopathies / pathology*
  • Leukoencephalopathies / physiopathology
  • Leukoencephalopathies / therapy
  • Magnetic Resonance Imaging
  • Male
  • Mutation*
  • Receptor, Macrophage Colony-Stimulating Factor / genetics*

Substances

  • Receptor, Macrophage Colony-Stimulating Factor

Supplementary concepts

  • Hereditary Diffuse Leukoencephalopathy with Spheroids