A rare case of hereditary sensory and autonomic neuropathy type II

Elmira Mamytova; Asel Jusupova; Anara Toktomametova; Kunduz Karbozova; Begimay Kadyrova; Yethindra Vityala; Tugolbai Tagaev

doi:10.1002/ccr3.7015

A rare case of hereditary sensory and autonomic neuropathy type II

Clin Case Rep. 2023 Mar 2;11(3):e7015. doi: 10.1002/ccr3.7015. eCollection 2023 Mar.

Authors

Elmira Mamytova¹, Asel Jusupova¹, Anara Toktomametova¹, Kunduz Karbozova¹, Begimay Kadyrova², Yethindra Vityala³, Tugolbai Tagaev⁴

Affiliations

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

We 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.

Keywords: arthrodesis; auto‐amputation; electromyography; fistula; hereditary sensory and autonomic neuropathy; osteomyelitis.

Publication types

Case Reports