Cleidorhizomelic syndrome: A very rare inherited syndrome mainly involving skeletal abnormalities. More detailed information about the symptoms, causes, and treatments of Cleidorhizomelic syndrome is available below.
Read more about symptoms of Cleidorhizomelic syndrome
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Read more about causes of Cleidorhizomelic syndrome.
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Choosing the Best Hospital: More general information, not necessarily in relation to Cleidorhizomelic syndrome, on hospital performance and surgical care quality:
Types of Cleidorhizomelic syndrome
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Cleidorhizomelic syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Cleidorhizomelic syndrome, or a subtype of Cleidorhizomelic 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 Cleidorhizomelic syndrome as a "rare disease".
Source - Orphanet
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