Juberg-Hayward syndrome: A rare hereditary disorder characterized by a growth hormone deficiency as well as mouth and limb abnormalities. More detailed information about the symptoms, causes, and treatments of Juberg-Hayward syndrome is available below.
See full list of 11 symptoms of Juberg-Hayward syndrome
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Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Read more about symptoms of Juberg-Hayward syndrome
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Juberg-Hayward syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Juberg-Hayward syndrome, or a subtype of Juberg-Hayward syndrome,
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 Juberg-Hayward syndrome as a "rare disease".
Source - Orphanet
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