Conditions / Genetic

Alexander disease

info · Genetic · ICD-10: G31.86

A leukodystrophy that is characterized by the destruction of white matter and the formation of Rosenthal fibers consisting of abnormal clumps of protein that accumulate in astrocytes.

Signs and symptoms

  • Dysmetria
  • Ataxia
  • Babinski sign
  • Dysarthria
  • Palatal tremor
  • Abnormal dentate nucleus morphology
  • Fatigue
  • Microcoria
  • Pendular nystagmus
  • Drowsiness

Also known as: Alexander's disease