Конечностно-поясная мышечная дистрофия с аутосомно- доминантным типом наследования: пельвиофеморальная форма Лейдена–Мебиуса
https://doi.org/10.17650/2222-8721-2013-0-1-46-61
Аннотация
В статье рассматриваются современные подходы к клинико-лабораторной диагностике конечностно-поясной мышечной дистрофии с акцентом на аутосомно-доминантные формы заболевания. Авторами представлено собственное клиническое наблюдение случая с поздней диагностикой пельвиофеморальной формы конечностно-поясной мышечной дистрофии с аутосомно-доминантным типом наследования у пациентки 37 лет.
Об авторах
Н. А. ШнайдерРоссия
Т. Я. Николаева
Россия
Е. Н. Бороева
Россия
Г. М. Пшенникова
Россия
Н. В. Лугинов
Россия
Ю. С. Панина
Россия
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Рецензия
Для цитирования:
Шнайдер Н.А., Николаева Т.Я., Бороева Е.Н., Пшенникова Г.М., Лугинов Н.В., Панина Ю.С. Конечностно-поясная мышечная дистрофия с аутосомно- доминантным типом наследования: пельвиофеморальная форма Лейдена–Мебиуса. Нервно-мышечные болезни. 2013;(1):46-61. https://doi.org/10.17650/2222-8721-2013-0-1-46-61
For citation:
Shnayder N.A., Nikolayeva T.Ya., Boroeva E.N., Pshennikova G.M., Luginov N.V., Panina Yu.S. Autosomal dominant limb-girdle muscular dystrophy: Leyden–Möbius pelvifemoral form. Neuromuscular Diseases. 2013;(1):46-61. (In Russ.) https://doi.org/10.17650/2222-8721-2013-0-1-46-61