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

• Autores principales: Roopam Jariwal MS (Autor), Basel Shoua MD (Autor), Katayoun Sabetian MD (Autor), Piruthiviraj Natarajan MD (Autor), Everardo Cobos MD (Autor)
• Formato: Libro
• Publicado: SAGE Publishing, 2018-02-01T00:00:00Z.
• Materias: article
• Acceso en línea: Connect to this object online.

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...