Peroxisomal acyl-CoA oxidase deficiency

MONDO:0009919

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.

Also known as: ACOX1 deficiency, Pseudoadrenoleukodystrophy, peroxisomal acyl-CoA oxidase deficiency, pseudo-NALD, pseudo-neonatal adrenoleukodystrophy, Pseudoneonatal adrenoleukodystrophy, straight-chain acyl-Coa oxidase deficiency

27 clinical trials for this condition and its sub-types.

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