Catel-Manzke Syndrome: A rare genetic disorder characterized by a small jaw, cleft palate and an extra bone at the base of the pointer finger. More detailed information about the symptoms, causes, and treatments of Catel-Manzke Syndrome is available below.
See full list of 12 symptoms of Catel-Manzke Syndrome
Review possible medical complications related to Catel-Manzke Syndrome:
Research the causes of these diseases that are similar to, or related to, Catel-Manzke Syndrome:
See full list of 17 occasional symptoms of Catel-Manzke Syndrome
Read more about causes of Catel-Manzke Syndrome.
More information about causes of Catel-Manzke Syndrome:
Medical research articles related to Catel-Manzke Syndrome include:
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Visit our research pages for current research about Catel-Manzke Syndrome treatments.
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Catel-Manzke Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Catel-Manzke Syndrome, or a subtype of Catel-Manzke Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Catel-Manzke Syndrome as a "rare disease".
Source - Orphanet
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