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

• المؤلفون الرئيسيون: O. A. Klochkova (مؤلف), A. L. Kurenkov (مؤلف), A. M. Mamed'yarov (مؤلف)
• التنسيق: كتاب
• منشور في: Union of pediatricians of Russia, 2014-07-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

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...