Alpers' disease or Alpers' Progressive Infantile Poliodystrophy is a rare, progressive neurodegenerative disease of the brain. It is thought to be an autosomal recessive disorder and usually affects children under the age of 5. Convulsions mark the onset of the disease, followed by dementia, spasticity and monoclonus. The untreatable disease is fatal and patients usually die a few months after disease onset.
Last update:September 26, 2015 at 2:35:17 UTC