Glutaricaciduria I: A rare inherited enzyme deficiency disorder where deficiency of the glutaryl-CoA dehydrogenase enzyme results in dystonia, dyskinesia and sometimes mental retardation. More detailed information about the symptoms, causes, and treatments of Glutaricaciduria I is available below.
See full list of 13 symptoms of Glutaricaciduria I
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Review possible medical complications related to Glutaricaciduria I:
Research the causes of these diseases that are similar to, or related to, Glutaricaciduria I:
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Read more about symptoms of Glutaricaciduria I
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Glutaricaciduria I is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Glutaricaciduria I, or a subtype of Glutaricaciduria I,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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