3-methylglutaconic aciduria, type 1: A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine. More detailed information about the symptoms, causes, and treatments of 3-methylglutaconic aciduria, type 1 is available below.
See full list of 27 symptoms of 3-methylglutaconic aciduria, type 1
Review possible medical complications related to 3-methylglutaconic aciduria, type 1:
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Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Read more about causes of 3-methylglutaconic aciduria, type 1.
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Prognosis for 3-methylglutaconic aciduria, type 1: The majority of patients died from progressive heart failure or sudden cardiac death.
More about prognosis of 3-methylglutaconic aciduria, type 1
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list 3-methylglutaconic aciduria, type 1 as a "rare disease".
Source - Orphanet
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