Oto-palato-digital syndrome, type 2: A rare genetic disorder characterized by head, face, mouth and bone abnormalities. More detailed information about the symptoms, causes, and treatments of Oto-palato-digital syndrome, type 2 is available below.
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A syndrome involving craniofacial, oral, and osseous structures characterized by short stature, unusual facies, cleft palate, and multiple skeletal malformations. Craniofacial abnormalities are generally milder in carrier females than those in males. Psychomotor development is usually normal but some patients have been reported as mentally retarded. - (Source - Diseases Database)
Oto-palato-digital syndrome, type 2 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Oto-palato-digital syndrome, type 2, or a subtype of Oto-palato-digital syndrome, type 2,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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