Rare Diseases Symptoms Automatic Extraction

Late-onset presentation of pyruvate dehydrogenase deficiency.

[pyruvate dehydrogenase deficiency]

Two brothers presented in their mid-forties with movement disorders including atypical parkinsonism, choreiform movements, stereotypies, ataxia and dysarthria. Both brothers showed putaminal lucencies on imaging and, in the proband, a deficiency of the pyruvate dehydrogenase complex (PDHC) was found on skin fibroblast assay.

Diseases presenting "dysarthria" symptom

  • alexander disease
  • cadasil
  • cholangiocarcinoma
  • gm1 gangliosidosis
  • hydrocephalus with stenosis of the aqueduct of sylvius
  • kabuki syndrome
  • krabbe disease
  • locked-in syndrome
  • megacystis-microcolon-intestinal hypoperistalsis syndrome
  • pyruvate dehydrogenase deficiency

This symptom has already been validated