Glutaric acidemia type I
Other Names for this Disease
- GA 1
- Glutaric acidemia 1
- Glutaric acidemia type 1
- Glutaric aciduria 1
- Glutaryl-CoA dehydrogenase deficiency
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Glutaric acidemia type I is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.
Last updated: 3/18/2011
- Glutaric acidemia type I. Genetics Home Reference (GHR). 2007; http://www.ghr.nlm.nih.gov/condition/glutaric-acidemia-type-i. Accessed 3/18/2011.