Experience of observing patients with Duchenne myopathy

Duchenne muscular dystrophy is a genetically determined fatal disease with a steadily progressive course. It is characterized by the absence or sharp decrease (less than 3 % of the norm) of the dystrophin protein. In recent years, several drugs for pathogenetic treatment of Duchenne myodystrophy hav...

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Bibliographic Details
Main Authors: L. I. Minaycheva, E. Yu. Petlina, E. G. Ravzhaeva, G. N. Seitova
Format: Article
Language:Russian
Published: ABV-press 2023-12-01
Series:Русский журнал детской неврологии
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Online Access:https://rjdn.abvpress.ru/jour/article/view/444
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