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Guillain-Barré Syndrome: Clinical Case

https://doi.org/10.24412/2790-1289-2023-4-28-34

Abstract

Guillain-Barré syndrome (GBS) is a paralytic peripheral neuropathy with an annual incidence of 0.81 to 1.89 cases (median: 1.11) per 100,000 people worldwide. The in-hospital mortality rate from GBS is approximately 2.6-2.8%. Risk factors include the severity of weakness at admission, time to reach maximum disability, the need for mechanical ventilation (MV), advanced age, as well as the presence of pulmonary and cardiac complications. Positive treatment outcomes are presented for one of the most common acute polyneuropathies—acute inflammatory polyradiculoneuropathy of autoimmune origin, or
Guillain-Barré syndrome. The pathomorphology is described in detail, the characteristics of various clinical variants are provided, and the diagnostic criteria and treatment methods for Guillain-Barré syndrome are presented. A case of acute inflammatory demyelinating polyradiculoneuropathy with the development of lower paraparesis is described. Clinical improvement was noted from the third day, and complete recovery of neurological deficits, both clinically and according to ENMG data, was observed after 3 months.

About the Authors

K. Z. Shamsiddinova
NEI «Kazakh-Russian Medical University»
Kazakhstan

Shamsiddinova Kamila Zarbitdinovna – second-year resident

Almaty



D. N. Mazhit
NEI «Kazakh-Russian Medical University»
Kazakhstan

Mazhit Nursultan Duisebaiuly – second-year resident

Almaty



M. M. Lepesova
NEI «Kazakh-Russian Medical University»
Kazakhstan

Lepesova Marzhan Makhmutovna – Doctor of Medical Sciences, Professor, Head of the Neurology Department

Almaty



M. A. Kazhaubaeva
NEI «Kazakh-Russian Medical University»
Kazakhstan

Kazhaubaeva Manchuk Amantaevna – Assistant Professor of Neurology

Almaty



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Review

For citations:


Shamsiddinova K.Z., Mazhit D.N., Lepesova M.M., Kazhaubaeva M.A. Guillain-Barré Syndrome: Clinical Case. Actual Problems of Theoretical and Clinical Medicine. 2023;(4):28-35. (In Russ.) https://doi.org/10.24412/2790-1289-2023-4-28-34

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ISSN 2790-1289 (Print)
ISSN 2790-1297 (Online)