Митохондриальные кардиомиопатии


https://doi.org/10.21508/1027-4065-2016-61-3-22-30

Полный текст:


Аннотация

Рассмотрена проблема диагностики гетерогенных форм митохондриальных кардиомиопатий, связанных с нарушением окислительного фосфорилирования и снижением активности митохондриальной электронно-транспортной системы вследствие мутации генов митохондриальной или ядерной ДНК. Подчеркнуто, что митохондриальные кардиомиопатии редко представляют изолированное поражение миокарда, чаще служат проявлением мультисистемного заболевания. Дана характеристика кардиомиопатии при отдельных митохондриальных синдромах, отражены возможности лечения патологии.

Об авторах

И. В. Леонтьева
ОСП «Научно-исследовательский клинический институт педиатрии им. Ю.Е. Вельтищева» ГБОУ ВПО РНИМУ им. Н.И. Пирогова
Россия

д.м.н., проф., гл. н. сотр. отдела детской кардиологии и аритмологии,

125412 Москва, ул. Талдомская, д.2



Е. А. Николаева
ОСП «Научно-исследовательский клинический институт педиатрии им. Ю.Е. Вельтищева» ГБОУ ВПО РНИМУ им. Н.И. Пирогова
Россия

д.м.н., и.о. рук. отдела психоневрологии и наследственных заболеваний,

125412 Москва, ул. Талдомская, д.2



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Дополнительные файлы

Для цитирования: Леонтьева И.В., Николаева Е.А. Митохондриальные кардиомиопатии. Российский вестник перинатологии и педиатрии. 2016;61(3):22-30. https://doi.org/10.21508/1027-4065-2016-61-3-22-30

For citation: Leontyeva I.V., Nikolaeva E.A. Mitochondrial cardiomyopathies. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2016;61(3):22-30. (In Russ.) https://doi.org/10.21508/1027-4065-2016-61-3-22-30

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