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Pyknoachondrogenesis: A very rare lethal syndrome characterized mainly by abnormal skeletal growth as well as abnormal bone calcification. More detailed information about the symptoms, causes, and treatments of Pyknoachondrogenesis is available below.
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Read more about causes of Pyknoachondrogenesis.
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Pyknoachondrogenesis is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Pyknoachondrogenesis, or a subtype of Pyknoachondrogenesis,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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