Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia: A rare syndrome characterized by a hand deformity and skeletal abnormalities. More detailed information about the symptoms, causes, and treatments of Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia is available below.
See full list of 13 symptoms of Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia
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Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia, or a subtype of Camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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