Stickler Syndrome, type III: A rare genetic disorder characterized by joint problems, distinctive facial characteristics and ear abnormalities. Type 3 is caused by a genetic defect on chromosome 6q21.3. Type 3 doesn't involve any of the eye problems that occur in type 1 and 2. More detailed information about the symptoms, causes, and treatments of Stickler Syndrome, type III is available below.
See full list of 38 symptoms of Stickler Syndrome, type III
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See full list of 8 occasional symptoms of Stickler Syndrome, type III
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