Schinzel Giedion Syndrome: A rare genetic disorder characterized by many skeletal and genital anomalies, unusual face, mental retardation and kidney malformations. More detailed information about the symptoms, causes, and treatments of Schinzel Giedion Syndrome is available below.
See full list of 63 symptoms of Schinzel Giedion Syndrome
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See full list of 10 occasional symptoms of Schinzel Giedion Syndrome
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Types of Schinzel Giedion Syndrome
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Schinzel Giedion Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Schinzel Giedion Syndrome, or a subtype of Schinzel Giedion Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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