A rare case of hereditary sensory and autonomic neuropathy type II

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 pr...

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Autores principales: Mamytova, Elmira, Jusupova, Asel, Toktomametova, Anara, Karbozova, Kunduz, Kadyrova, Begimay, Vityala, Yethindra, Tagaev, Tugolbai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981577/
https://www.ncbi.nlm.nih.gov/pubmed/36873073
http://dx.doi.org/10.1002/ccr3.7015
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author Mamytova, Elmira
Jusupova, Asel
Toktomametova, Anara
Karbozova, Kunduz
Kadyrova, Begimay
Vityala, Yethindra
Tagaev, Tugolbai
author_facet Mamytova, Elmira
Jusupova, Asel
Toktomametova, Anara
Karbozova, Kunduz
Kadyrova, Begimay
Vityala, Yethindra
Tagaev, Tugolbai
author_sort Mamytova, Elmira
collection PubMed
description 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.
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spelling pubmed-99815772023-03-04 A rare case of hereditary sensory and autonomic neuropathy type II Mamytova, Elmira Jusupova, Asel Toktomametova, Anara Karbozova, Kunduz Kadyrova, Begimay Vityala, Yethindra Tagaev, Tugolbai Clin Case Rep Case Report 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. John Wiley and Sons Inc. 2023-03-02 /pmc/articles/PMC9981577/ /pubmed/36873073 http://dx.doi.org/10.1002/ccr3.7015 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Mamytova, Elmira
Jusupova, Asel
Toktomametova, Anara
Karbozova, Kunduz
Kadyrova, Begimay
Vityala, Yethindra
Tagaev, Tugolbai
A rare case of hereditary sensory and autonomic neuropathy type II
title A rare case of hereditary sensory and autonomic neuropathy type II
title_full A rare case of hereditary sensory and autonomic neuropathy type II
title_fullStr A rare case of hereditary sensory and autonomic neuropathy type II
title_full_unstemmed A rare case of hereditary sensory and autonomic neuropathy type II
title_short A rare case of hereditary sensory and autonomic neuropathy type II
title_sort rare case of hereditary sensory and autonomic neuropathy type ii
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9981577/
https://www.ncbi.nlm.nih.gov/pubmed/36873073
http://dx.doi.org/10.1002/ccr3.7015
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