Unmasking a Case of Asymptomatic Charcot-Marie-Tooth Disease (CMT1A) With Vincristine

Charcot-Marie-Tooth (CMT) disease is a hereditary demyelinating disease of the peripheral nervous system that results in sensory and motor dysfunction. CMT includes a spectrum of diseases with different types of mutations in the genes encoding myelin protein, resulting in a variety of dysfunctions i...

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Detalles Bibliográficos
Autores principales: Jariwal, Roopam, Shoua, Basel, Sabetian, Katayoun, Natarajan, Piruthiviraj, Cobos, Everardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833168/
https://www.ncbi.nlm.nih.gov/pubmed/29511693
http://dx.doi.org/10.1177/2324709618758349

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833168/
https://www.ncbi.nlm.nih.gov/pubmed/29511693
http://dx.doi.org/10.1177/2324709618758349

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