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of the North Caucasus
Scientific journal
Mass media registration certificate dated December 7, 2006.
Series ПИ #ФС 77-26521.
Federal service for surveillance over non-violation of the legislation in the sphere of mass communications and protection of cultural heritage.
ISSN 2073-8137
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Dilated cardiomyopathy in patient with the hereditary disease – Duchenne-Becker`s muscular dystrophy

[Notes from practice]
Alexandr Yagoda; Olga Boeva; Elena Scheglova; Natalya Bulgakova;

A clinical case of dilated cardiomyopathy in adult with progressing muscular dystrophy has been presented. The disease manifested by severe heart failure.

Authors consider including echocardiography in the list of routine diagnostic procedures for children with Duchenne’s or Becker’s muscular dystrophy for early revealing of cardiac involvement. The long-term ambulatory observation by cardiologist is also recommended in spite of absence of heart pathology signs.

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Keywords: Duchenne muscular dystrophy, Becker muscular dystrophy, cardiomyopathy


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