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Tel Hashomer Camptodactyly Syndrome: Report on a New Case

Rafaela Nicolau1,2, Cristina Rodrigues3, Tiago Beirão4

  • 1Rheumatology Department, Centro Hospitalar Tondela-Viseu, Viseu, Portugal.

International Journal of Rheumatic Diseases
|March 26, 2025
PubMed
Abstract

No abstract available in PubMed .

Keywords:
Tel Hashomer syndromecamptodactylyskeletal dysplasia

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Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...

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