Open AccessClinical features of cardiomiopathies caused by cardiac troponin I mutations (review)
Author(s) -
M. V. Youschenko,
E. V. Shlyakhto,
Г. А. Новик,
Anna Kostareva,
А. Я. Гудкова
Publication year - 2009
Publication title -
arterialʹnaâ gipertenziâ
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.126
H-Index - 5
eISSN - 2411-8524
pISSN - 1607-419X
DOI - 10.18705/1607-419x-2009-15-6-648-651
Subject(s) - troponin , cardiology , medicine , hypertrophic cardiomyopathy , sudden cardiac death , phenotype , mutation , troponin i , genetics , biology , gene , myocardial infarction
Clinical and genetic aspects of cardiomyopathies caused by cardiac troponin I mutations are observed. Apparent clinical heterogeneity with development of both hypertrophic and restrictive phenotypes and high risk of sudden death are presented.