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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Detalles Bibliográficos
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

Internet

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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