A rare case of hereditary sensory and autonomic neuropathy type II

A rare case of hereditary sensory and autonomic neuropathy type II

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 unfav...

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Podrobná bibliografie
Hlavní autoři: Elmira Mamytova, Asel Jusupova, Anara Toktomametova, Kunduz Karbozova, Begimay Kadyrova, Yethindra Vityala, Tugolbai Tagaev
Médium: Článek
Jazyk:English
Vydáno: Wiley 2023-03-01
Edice:Clinical Case Reports
Témata:
arthrodesis
auto‐amputation
electromyography
fistula
hereditary sensory and autonomic neuropathy
osteomyelitis
On-line přístup:https://doi.org/10.1002/ccr3.7015

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