Редкие клинические случаи: сочетание некомпактной кардиомиопатии с аномалией Эбштейна

DOI: https://doi.org/10.29296/25877305-2019-12-11
Номер журнала: 
12
Год издания: 
2019

С. Комиссарова(1), доктор медицинских наук, Н. Ринейская(1), Т. Севрук(1), И. Гайдель1, Н. Чакова(2), кандидат биологических наук, С. Ниязова(2) 1-Республиканский научно-практический центр «Кардиология», Минск, Республика Беларусь 2-Институт генетики и цитологии НАН Беларуси, Минск, Республика Беларусь E-mail: nadya.rin@gmail.com

Представлены редкие клинические случаи сочетания аномалии Эбштейна с некомпактной кардиомиопатией, синдромом Вольфа–Паркинсона–Уайта, ассоциированные с мутациями в гене MYH7. Обсуждаются вопросы диагностики, особенности клинических проявлений и тактики ведения пациентов с данной патологией.
Ключевые слова: 
кардиология, некомпактная кардиомиопатия, аномалия Эбштейна, синдром Вольфа–Паркинсона–Уайта, саркомерные гены, мутации в гене MYH7

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