Glutaric aciduria I (medical condition): A rare inherited enzyme deficiency disorder where deficiency of the glutaryl-CoA dehydrogenase enzyme results in dystonia, dyskinesia and sometimes mental retardation.
See also:
Glutaricaciduria I:
»Introduction: Glutaricaciduria I
»Symptoms of Glutaricaciduria I
These medical condition or symptom topics may be relevant to medical information for Glutaric aciduria I:
Glutaric aciduria I is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Glutaric aciduria I, or a subtype of Glutaric aciduria I,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Glutaric aciduria I (medical condition): See Glutaricaciduria I (disease information).
»Introduction: Glutaricaciduria I
»Symptoms of Glutaricaciduria I
These medical disease topics may be related to Glutaric aciduria I:
Source - NIH
Search to find out more about Glutaric aciduria I:
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