CARDIOMYOPATHY IN THE FRIEDREICH ATAXIA: CLINICAL PRESENTATION AND DIAGNOSTICS OF COMPLICATIONS

Friedreich’s ataxia (FA) is one of the most prevalent variants of the inherited ataxias. The disease is characterized by complicated phenotype that includes neurological signs (ataxia, sensory polyneuropathy, dysarthria, disorders of deep sensitivity, areflexia, pyramid symptoms with lower extremiti...

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Main Authors:	Е. I. Fomicheva, R. P. Myasnikov, Yu. A. Selivyorstov, Е. L. Dadali, Yu. Yu. Kotalevskaya, М. S. Kharlap, S. N. Koretsky, Е. P. Nuzhny, Е. А. Mershina, V. Е. Sinitsyn, А. N. Vernokhaeva, Е. V. Bazaeva, О. М. Drapkina, S. А. Boytsov
Format:	Article
Language:	Russian
Published:	«FIRMA «SILICEA» LLC 2017-11-01
Series:	Российский кардиологический журнал
Subjects:	friedreich cardiomyopathy friedreich ataxia cardiomyopathies myocardial hypertrophy heart failure sudden cardiac death non-compaction myocardium of the left ventricle
Online Access:	https://russjcardiol.elpub.ru/jour/article/view/2530

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https://russjcardiol.elpub.ru/jour/article/view/2530

CARDIOMYOPATHY IN THE FRIEDREICH ATAXIA: CLINICAL PRESENTATION AND DIAGNOSTICS OF COMPLICATIONS

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