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Fumaric aciduria
rareFumaric aciduria (FA), an autosomal recessive metabolic disorder, is most often characterized by early onset but non-specific clinical signs: hypotonia, severe psychomotor impairment, convulsions, respiratory distress, feeding difficulties and frequent cerebral malformations, along with a distinctive facies. Some patients present with only moderate intellectual impairment.
- Identifiers
- MONDO:0011730 OMIM:606812Orphanet:24
- Causal genes
- FH
- Part of
- Hereditary peripheral neuropathyInborn mitochondrial metabolism disorderTricarboxylic acid cycle disorder
- Also known as
- FMRD · fumarase deficiency · fumarate hydratase deficiency
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