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Tel-Hashomer camptodactyly syndrome

Tel-Hashomer camptodactyly syndrome: Introduction

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.

Symptoms of Tel-Hashomer camptodactyly syndrome

Wrongly Diagnosed with Tel-Hashomer camptodactyly syndrome?

Tel-Hashomer camptodactyly syndrome: Related Patient Stories

Tel-Hashomer camptodactyly syndrome: Complications

Read more about complications of Tel-Hashomer camptodactyly syndrome.

Causes of Tel-Hashomer camptodactyly syndrome

Read more about causes of Tel-Hashomer camptodactyly syndrome.

Misdiagnosis and Tel-Hashomer camptodactyly syndrome

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Tel-Hashomer camptodactyly syndrome: Research Doctors & Specialists

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Tel-Hashomer camptodactyly syndrome: Animations

Statistics for Tel-Hashomer camptodactyly syndrome

Tel-Hashomer camptodactyly syndrome: Broader Related Topics

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Definitions of Tel-Hashomer camptodactyly syndrome:

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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