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Isovaleric Acidemia
Isovaleric Acidemia: Introduction
Isovaleric Acidemia: A condition which is characterized by a defect in the pathway of leucine catabolism. More detailed information about the symptoms, causes, and treatments of Isovaleric Acidemia is available below.
Evidence Based Medicine Research for Isovaleric Acidemia
Medical research articles related to Isovaleric Acidemia include:
- Inborn Errors of Metabolism in Infancy and Early Childhood: An Update
- Carnitine Deficiency (Diagnosis)
- Hyperammonemia (Overview)
- Hyperammonemia (Diagnosis)
- Carnitine Deficiency (Treatment)
- Carnitine Deficiency (Follow-up)
- Hyperammonemia (Treatment)
- Carnitine Deficiency (Overview)
- more research...»
Click here to find more evidence-based articles on the TRIP Database
Videos for Isovaleric Acidemia
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Reseach about Isovaleric Acidemia
Visit our research pages for current research about Isovaleric Acidemia treatments.
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Definitions of Isovaleric Acidemia:
Isovaleric Acidemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Isovaleric Acidemia, or a subtype of Isovaleric Acidemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Isovaleric Acidemia as a "rare disease".
Source - Orphanet
» Next page: What is Isovaleric Acidemia?
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- Prevalence and Incidence of Isovaleric Acidemia
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