Antley-Bixler Syndrome: A rare genetic disorder characterized by premature closing of skull bones, choanal atresia and craniofacial and limb abnormalities. More detailed information about the symptoms, causes, and treatments of Antley-Bixler Syndrome is available below.
See full list of 26 symptoms of Antley-Bixler Syndrome
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See full list of 12 occasional symptoms of Antley-Bixler Syndrome
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Types of Antley-Bixler Syndrome
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Antley-Bixler Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Antley-Bixler Syndrome, or a subtype of Antley-Bixler 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 Antley-Bixler Syndrome as a "rare disease".
Source - Orphanet
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