Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report

BACKGROUND: HINT1 mutations cause an autosomal recessive axonal neuropathy with neuromyotonia. This is a first case report of coexistence of myasthenia gravis (MG) and HINT1-related motor axonal neuropathy without neuromyotonia. CASE PRESENTATION: A 32-year-old woman presented with recurrent ptosis...

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Detalles Bibliográficos
Autores principales: Fang, Jia, Huang, Hui, Lei, Qiang, Luo, Yingying, Tang, Zhengchu, Shi, Xiaoliu, Tang, Jian Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063049/
https://www.ncbi.nlm.nih.gov/pubmed/35501818
http://dx.doi.org/10.1186/s12883-022-02690-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063049/
https://www.ncbi.nlm.nih.gov/pubmed/35501818
http://dx.doi.org/10.1186/s12883-022-02690-6

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