Hay-Wells Syndrome: A rare genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate. More detailed information about the symptoms, causes, and treatments of Hay-Wells Syndrome is available below.
See full list of 29 symptoms of Hay-Wells Syndrome
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See full list of 12 occasional symptoms of Hay-Wells Syndrome
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Types of Hay-Wells Syndrome
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Hay-Wells Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hay-Wells Syndrome, or a subtype of Hay-Wells 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 Hay-Wells Syndrome as a "rare disease".
Source - Orphanet
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