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Camptomelic syndrome: A rare inherited skeletal disorder characterized by short stature, missing ribs and other abnormalities. More detailed information about the symptoms, causes, and treatments of Camptomelic syndrome is available below.
Read more about causes of Camptomelic syndrome.
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Camptomelic syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Camptomelic syndrome, or a subtype of Camptomelic syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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