Hay-Wells syndrome, recessive type: A rare recessively inherited genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate. The recessive form of this condition is distinguished by the presence at birth of adhesions between the upper and lower jaws. More detailed information about the symptoms, causes, and treatments of Hay-Wells syndrome, recessive type is available below.
See full list of 24 symptoms of Hay-Wells syndrome, recessive type
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Hay-Wells syndrome, recessive type 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, recessive type, or a subtype of Hay-Wells syndrome, recessive type,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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