Stickler Syndrome, type II: A rare genetic disorder characterized by joint problems, distinctive facial characteristics and eye and ear abnormalities. Type 2 is caused by a genetic defect on chromosome 1p21. More detailed information about the symptoms, causes, and treatments of Stickler Syndrome, type II is available below.
See full list of 43 symptoms of Stickler Syndrome, type II
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See full list of 10 occasional symptoms of Stickler Syndrome, type II
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