3-Hydroxyisobutyric aciduria
3-Hydroxyisobutyric aciduria: Introduction
3-Hydroxyisobutyric aciduria: A rare inborn metabolic disorder which causes brain and facial anomalies, seizures and growth problems.
More detailed information about the symptoms,
causes, and treatments of 3-Hydroxyisobutyric aciduria is available below.
Symptoms of 3-Hydroxyisobutyric aciduria
See full list of 19
symptoms of 3-Hydroxyisobutyric aciduria
Medical Textbooks Online about 3-Hydroxyisobutyric aciduria
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Wrongly Diagnosed with 3-Hydroxyisobutyric aciduria?
Causes of 3-Hydroxyisobutyric aciduria
Read more about causes of 3-Hydroxyisobutyric aciduria.
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Definitions of 3-Hydroxyisobutyric aciduria:
3-Hydroxyisobutyric aciduria is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that 3-Hydroxyisobutyric aciduria, or a subtype of 3-Hydroxyisobutyric aciduria,
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 3-Hydroxyisobutyric aciduria as a "rare disease".
Source - Orphanet
Contents for 3-Hydroxyisobutyric aciduria:
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