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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Main Authors: | , , , |
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Format: | Article |
Language: | Russian |
Published: |
ABV-press
2023-12-01
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Series: | Русский журнал детской неврологии |
Subjects: | |
Online Access: | https://rjdn.abvpress.ru/jour/article/view/444 |
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