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