Fumaric aciduria

Fumaric 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.

Also known as: fumarase deficiency, fumaric aciduria, FMRD, fumarate hydratase deficiency

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