4.2 Article

Genetic Infiltrative Cardiomyopathies

期刊

HEART FAILURE CLINICS
卷 14, 期 2, 页码 215-224

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.hfc.2017.12.003

关键词

Amyloidosis; Hemochromatosis; Cardiac oxalosis; Friedreich ataxia; Mucopolysaccharidosis; Fabry disease; Danon disease; PRKAG2 syndrome

资金

  1. NHLBI NIH HHS [R01 HL147064, R01 HL109209] Funding Source: Medline

向作者/读者索取更多资源

Infiltrative cardiomyopathies are characterized by abnormal accumulation or deposition of substances in cardiac tissue leading to cardiac dysfunction. These can be inherited, resulting from mutations in specific genes, which engender a diverse array of extracardiac features but overlapping cardiac phenotypes. This article provides an overview of each inherited infiltrative cardiomyopathy, describing the causative genes, the pathologic mechanisms involved, the resulting cardiac manifestations, and the therapies currently offered or being developed.

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