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When rare illuminates common: how cardiocutaneous syndromes transformed our perspective on arrhythmogenic cardiomyopathy.
Sen-Chowdhry, Srijita; McKenna, William J.
Afiliación
  • Sen-Chowdhry S; Inherited Cardiovascular Disease Group, Institute of Cardiovascular Science, University College London , UK.
Cell Commun Adhes ; 21(1): 3-11, 2014 Feb.
Article en En | MEDLINE | ID: mdl-24460197
The classic cardiocutaneous syndromes of Naxos and Carvajal are rare. The myocardial disorder integral to their pathology - arrhythmogenic cardiomyopathy - is arguably not uncommon, with a prevalence of up to 1 in 1,000 despite almost certain under-recognition. Yet the study of cardiocutaneous syndromes has been integral to evolution of the contemporary perspective of arrhythmogenic cardiomyopathy - its clinical course, disease spectrum, genetics, and cellular and molecular mechanisms. Here we discuss how recognition of the association of hair and skin abnormalities with underlying heart disease transformed our conception of a little-understood but important cause of sudden cardiac death.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Displasia Ventricular Derecha Arritmogénica / Síndrome LEOPARD Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Cell Commun Adhes Año: 2014 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Displasia Ventricular Derecha Arritmogénica / Síndrome LEOPARD Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: Cell Commun Adhes Año: 2014 Tipo del documento: Article