CLINICAL AND DIAGNOSTIC FEATURES OF ATYPICAL FORMS OF PROGRESSIVE MUSCULAR DUSHEN DYSTROPHY

Authors

  • Djurabekova Aziza Taxirovna Doctor of Medical Sciences, Prof. Head of the Department of Neurology and Neurosurgery, Samarkand State Medical Institute
  • Bazarova Aziza Kobiljojovna Assistant at the Department of Neurology Samarkand State Medical Institute
  • Raximova Amira Rustamovna Clinical Resident of the Department of Neurology Samarkand State Medical Institute

Keywords:

disease, neuromuscular, congenital, myopathy, diagnosis

Abstract

Among the hereditary groups of the disease, neuromuscular diseases are considered the
most common. The disease is complex, differential diagnosis, especially congenital myopathy.
Common signs of congenital structural myopathies are early onset, skeletal anomaly, generalized
muscle hypotension, and severe complications from the cardiovascular system and respiratory
tract. Statistical data The incidence of progressive Duchenne muscular dystrophy (PMDD) varies
from 10 to 33 per 100 thousand boys in the general population

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Published

2021-04-17

Issue

2021: 4th GCCSA

Section

Articles

License

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.