Clinical-Electroneuromyographic Characteristics of The Patients with Duchenne/Becker’s Progressive Muscular Dystrophy in Uzbekistan

Authors

  • Yo.N. Madjidova Tashkent Pediatric Medical Institute, Department of Neurology, Child neurology and Medical Genetics, Tashkent, Uzbekistan
  • U.T. Omonova Tashkent Pediatric Medical Institute, Department of Neurology, Child neurology and Medical Genetics, Tashkent, Uzbekistan

DOI:

https://doi.org/10.61788/njn.v1i15.07

Keywords:

Duchenne’s myodystrophy, Becker’s myodystrophy, clinical polymorphism

Abstract

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References

Zinchenko R.A. Epidemiology of hereditary diseases in Russian populations. Abstract of diss. for Doct. of med.sci. - M. - 2001.-46p.

Kirilenko N.B. Features of nosological spectrum and clinical characteristics of hereditary diseases of nervous system in cities of Volgograd and Volgskiy. Abstract. Of diss. for Cand. med.sci.- M.- 2005-26p.

Koren O.L. Prevalence and clinical polymorphism of hereditary diseases with disorders of nervous system in Novokuznetsk. Abstract of diss. for Cand.med.sci.- M. - 2005.-24p.

Krakhmaleva I.N., Lipatova N., Shishkin S.S., Shakhovskaya N.I. Structure of the dystrophin gene in patients with Duchenne’s myodystrophy. Jurn. Nevropatologii i psychiatrii, 1999, N 3: 41.

Rakhmonov R.A. Hereditary diseases of nervous system in Tadjikistan. Abstract of diss. for Doct. med.sci. -М.-2004. - 44 p.

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Published

30.06.2015

How to Cite

Madjidova, Y., & Omonova, U. (2015). Clinical-Electroneuromyographic Characteristics of The Patients with Duchenne/Becker’s Progressive Muscular Dystrophy in Uzbekistan. National Journal of Neurology, 43–45. https://doi.org/10.61788/njn.v1i15.07

Issue

2015: No.1 (7)

Section

Original Articles

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