Hypertelorism with esophageal abnormality and hypospadias: A congenital disorder characterized by distinctive facial features, genital abnormalities, esophageal defect and difficulty swallowing. Males are more severely affected than females. More detailed information about the symptoms, causes, and treatments of Hypertelorism with esophageal abnormality and hypospadias is available below.
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Prognosis for Hypertelorism with esophageal abnormality and hypospadias: The prognosis varies depending on the type and severity of the symptoms which can vary considerably amongst patients. Prognosis and quality of life can be improved by appropriate treatment and monitoring. Most patients have a normal life span and normal growth.
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Hypertelorism with esophageal abnormality and hypospadias is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hypertelorism with esophageal abnormality and hypospadias, or a subtype of Hypertelorism with esophageal abnormality and hypospadias,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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