A rare case of hereditary sensory and autonomic neuropathy type II

Author:

Mamytova Elmira1,Jusupova Asel1,Toktomametova Anara1,Karbozova Kunduz1,Kadyrova Begimay2,Vityala Yethindra3ORCID,Tagaev Tugolbai4

Affiliation:

1. A.N. Murzaliev Department of Neurology and Clinical Genetics I.K. Akhunbaev Kyrgyz State Medical Academy Bishkek Kyrgyzstan

2. Department of Special Clinical Disciplines International Higher School of Medicine Bishkek Kyrgyzstan

3. Department of Pathology International Higher School of Medicine Bishkek Kyrgyzstan

4. Department of Public Health and Healthcare I. K. Akhunbaev Kyrgyz State Medical Academy Bishkek Kyrgyzstan

Abstract

AbstractWe describe the follow‐up of a 29‐year‐old man diagnosed with hereditary sensory and autonomic neuropathy type II, including the different complications that presented since his childhood. Despite efforts to maintain an optimal quality of life, the lack of an early diagnosis led to an unfavorable prognosis and life condition.

Publisher

Wiley

Subject

General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Phenotypic features of RETREG1‐related hereditary sensory autonomic neuropathy;Journal of the Peripheral Nervous System;2023-07-24

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