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КЛИНИЧЕСКИЕ ОСОБЕННОСТИ И МОЛЕКУЛЯРНОГЕНЕТИЧЕСКИЕ МЕХАНИЗМЫ РАЗВИТИЯ ЦЕРЕБРАЛЬНЫХ ИНСУЛЬТОВ У ДЕТЕЙ

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АННОТАЦИЯ СТАТЬИ

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Церебро-васкулярная патология является одной из интереснейших и изучаемых проблем в детской неврологии, актуальность которой определяется высокой степенью инвалидизации и смертности детей различных возрастных групп. Уровень мировой медицины вышел на ступень генетических исследований, исключающих или подтверждающих наличие мутации в генах. Среди многих причин инсультов у детей называлась и генетическая предрасположенность [Simma 2010.; Zadro 2012; Balcerzyk, 2018], отмеченная и среди взрослых больных с инсультами [Tan 2018]. В данной статье предоставляется современный обзор зарубежной литературы посвящённый вопросам этиологии,классификации, клиники и молекулярно-генетических исследований в области детской инсультологии. Выводы показали, что выявление генов кандидатов, формирующих предрасположенность к инсульту, представляет одну из приоритетных задач для исследователей этой проблемы.

АВТОРЫ

S.Nazarova

SH.Shamansurov

Теги

# дети# children# болалар# ischemic stroke# hemorrhagic stroke# ишемик инсульт# геморрагик инсульт# ишемический инсульт# геморрагический инсульт# gene# гомоцистеин# homocysteine# ген

ДРУГИЕ СТАТЬИ ЭТОГО ЖУРНАЛА

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Список литературы

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