Синдром Прадера-Вилли: новые возможности в лечении детей

Синдром Прадера-Вилли (СПВ) представляет собой генетическое заболевание, главными симптомами которого являются тяжелая гиперфагия, приводящая к выраженному ожирению, задержка роста, характерные внешние особенности, сложности в обучении, поведенческие и психиатрические проблемы. В настоящее время единственным эффективным средством лечения СПВ, значительно улучшающим качество жизни пациентов, является рекомбинантный гормон роста (р-ГР). Проведен анализ многочисленных положительных эффектов и возможных рисков терапии р-ГР при СПВ.

синдром Прадера-Вилли, задержка роста, ожирение, композиционный состав тела, гормон роста, апноэ

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