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Cardiomyopathy III: Hypertrophic Cardiomyopathy

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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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Dissecting idiopathic multicentric Castleman's disease

Nicolas Dupin¹

¹Service de Dermatologie, Hôpital Cochin, APHP and Université Paris Descartes, Institut Cochin INSERM U1016, Paris 75006, France.

The Lancet. Haematology

|April 12, 2016

Summary

No abstract available in PubMed .

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