13 top medical experts on Peroxisomal ACYL-COA oxidase deficiency across 0 countries. This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Peroxisomal ACYL-COA oxidase deficiency: Peroxisomal acyl-CoA oxidase deficiency is a rare neurodegenerative disorder that belongs to the group of inherited peroxisomal disorders and is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Organizations Providing General Support

  • Synonyms: Pseudoneonatal adrenoleukodystrophy,  Straight-chain ACYL-COA oxidase deficiency


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