Clinical-electroneuromyographic characteristics of the patients with duchenne/becker's progressive muscular dystrophy in Uzbekistan

We examined 106 patients with a diagnosis of Duchenne / Becker progressive muscular dystrophy (PMD), selected in the group of those who applied to the Republican Center for Screening of Mother and Child with various hereditary neuromuscular diseases. Based on the analysis of pedigrees, clinical manifestations and paraclinical research methods, the features of the clinical polymorphism of this disease in Uzbekistan were studied.

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