Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary neurological disease · Inborn organic aciduria · Glutaric aciduria
Glutaryl-CoA dehydrogenase deficiency
Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder.
This condition has no sub-types.