Tel-Hashomer camptodactyly syndrome: A very rare syndrome characterized mainly by finger flexion, facial anomalies, short stature and muscle problems. More detailed information about the symptoms, causes, and treatments of Tel-Hashomer camptodactyly syndrome is available below.
See full list of 23 symptoms of Tel-Hashomer camptodactyly syndrome
Read more about complications of Tel-Hashomer camptodactyly syndrome.
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Tel-Hashomer camptodactyly syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Tel-Hashomer camptodactyly syndrome, or a subtype of Tel-Hashomer camptodactyly 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 Tel-Hashomer camptodactyly syndrome as a "rare disease".
Source - Orphanet
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