MEROSIN-DEFICIENT CONGENITAL MUSCULAR DYSTROPHY (CMD1A): CLINICAL CASE OF CONGENITAL MUSCULAR DYSTROPHY INVOLVING CENTRAL NERVOUS SYSTEM

Congenital muscular dystrophies (CMDs) are an extremely heterogenous group of neuromuscular diseases. The article presents the general information on clinical and pathogenetic aspects of CMD diagnosis with emphasis on one of the most common forms of nervous system disturbances — merosin-deficient co...

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Principais autores:	O. A. Klochkova, A. L. Kurenkov, A. M. Mamed'yarov
Formato:	Artigo
Idioma:	Russo
Publicado em:	Union of pediatricians of Russia 2014-07-01
coleção:	Педиатрическая фармакология
Assuntos:	congenital muscular dystrophy merosin-deficient muscular dystrophy cmd1a merosin lama2 floppy infant syndrome myopathies electromyography magnetic resonance imaging muscle biopsy creatine phosphokinase neuromuscular diseases
Acesso em linha:	https://www.pedpharma.ru/jour/article/view/77
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