КЛИНИЧЕСКИЙ СЛУЧАЙ ПОЗДНЕГО ПРОЯВЛЕНИЯ БОЛЕЗНИ ШАРКО-МАРИ- ТУТА_ (СЛУЧАЙ ИЗ ПРАКТИКИ)

Authors

  • Kasimova Sayyora Akmaljanovna
  • Kayumova Nafisa Kamiljanovna
  • Abduvaliyeva Gavhar Tulkunovna

Keywords:

neural amyotrophy, clinical case, SHarko Mari-Toot syndrome, hereditary polyneuropathy

Abstract

Medical genetics, being a relatively young science, remains the most urgent and demanding problem to this day. The largest percentage of this group is hereditary neuromuscular diseases, which are characterized by early onset, progressive course and quickly lead to disability and death. Sharko-Mari-Tuta   neural amyotrophy is a progressive hereditary disease with damage to the peripheral nervous system, leading to muscle atrophy of the distal parts of the arms and legs.

References

Федеральное руководство по Детской неврологии под редакцией В.И.Гузевой 2016г.

Н.П.Бочков Клиническая генетика 1997г.

С.И.Гончарова,Н.А.Шнайдер Наследственная невропатия Шарко-Мари-Тута:возможности нефармакологического лечения.Журнал «Физиология Бальнеология и реабилитация» 6/2013г.

Published

2024-09-26