Генетические факторы развития синдрома Майера—Рокитанского—Кюстера

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Под врожденными пороками развития понимают стойкие отклонения от нормы, морфологические и функциональные изменения органов и тканей, возникающие внутриутробно или после рождения. Пороки развития женских половых органов составляют 4% от всех аномалий развития. Зачастую диагностика отклонений развития гениталий сопровождается диагностическими ошибками в связи с большим разнообразием пороков и отсутствием единой классификации. В данном обзоре обобщены и представлены для обсуждения сведения о генетической предрасположенности к формированию одного из пороков развития — аплазии матки и влагалища.

Ключевые слова:

синдром Майера—Рокитанского—Кюстера—Хаузера

аплазия матки и влагалища

генетические аспекты

Авторы:

Аракелян А.С.

ФГБУ «Национальный медицинский исследовательский центр акушерства, гинекологии и перинатологии им. акад. В.И. Кулакова» Минздрава России

Попрядухин А.Ю.

Карапетян Э.А.

ФГАОУ ВО «Первый Московский государственный медицинский университет им. И.М. Сеченова» Минздрава России (Сеченовский Университет)

Даты поступления:

15.03.2020

Даты принятия в печать:

19.05.2020

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