Rare Diseases Symptoms Automatic Extraction

[Metabolic disorders with typical alterations in MRI].

[alexander disease]

The classification of metabolic disorders according to the etiology is not practical for neuroradiological purposes because the underlying defect does not uniformly transform into morphological characteristics. Therefore typical MR and clinical features of some easily identifiable metabolic disorders are presented. Canavan disease, Pelizaeus-Merzbacher disease, Alexander disease, X-chromosomal adrenoleukodystrophy and adrenomyeloneuropathy, mitochondrial disorders, such as MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes) and Leigh syndrome as well as L-2-hydroxyglutaric aciduria are presented.

Diseases presenting "aciduria" symptom

  • adrenomyeloneuropathy
  • alexander disease
  • canavan disease
  • child syndrome
  • classical phenylketonuria
  • cohen syndrome
  • cystinuria
  • homocystinuria without methylmalonic aciduria
  • neonatal adrenoleukodystrophy
  • phenylketonuria
  • primary hyperoxaluria type 1
  • pyruvate dehydrogenase deficiency
  • x-linked adrenoleukodystrophy

This symptom has already been validated