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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2023
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| Materias: | |
| 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 |