Tibial neuropathy, a rare manifestation of hereditary neuropathy with liability to pressure palsy: A case report

Hereditary neuropathy with liability to pressure palsy (HNPP) is characterized by acute, painless and recurrent mononeuropathies. Genetic testing shows PMP22 gene deletion of chromosome 17p11.2 can provide evidence for the diagnosis of HNPP. Reports on tibial neuropathy as the main manifestation of...

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Detalles Bibliográficos
Autores principales: Zhu, Geke, Nie, Xiangtao, Qi, Wenjing, Ma, Yongbo, Hao, Lei, Guo, Xiuming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372733/
https://www.ncbi.nlm.nih.gov/pubmed/37519674
http://dx.doi.org/10.1016/j.heliyon.2023.e18340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10372733/
https://www.ncbi.nlm.nih.gov/pubmed/37519674
http://dx.doi.org/10.1016/j.heliyon.2023.e18340

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