Clinical practice guidelines for the diagnosis and management of Charcot-Marie-Tooth disease

Charcot-Marie-Tooth disease (CMT) is classified according to neurophysiological and histological findings, the inheritance pattern, and the underlying genetic defect. The objective of these guidelines is to offer recommendations for the diagnosis, prognosis, follow-up, and treatment of this disease...

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Detalles Bibliográficos
Autores: Sivera Mascaró, R., García Sobrino, T., Horga Hernández, A., Pelayo Negro, A. L., Alonso Jiménez, A., Antelo Pose, A., Calabria Gallego, M.D., Casasnovas, Carlos, Cemillán Fernández, C.A., Gutiérrez Gutiérrez, Gerardo, Et. al.
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universidad Europea (UEM)
Repositorio:ABACUS. Repositorio de Producción Científica
Idioma:inglés
OAI Identifier:oai:abacus.universidadeuropea.com:11268/16859
Acceso en línea:https://hdl.handle.net/11268/16859
Access Level:acceso abierto
Palabra clave:Enfermedad de Charcot-Marie-Tooth
Neuropatía Hereditaria Motora y Sensorial
España
Enfermedad del sistema nervioso
Neurología
Medicina preventiva
Goal 3: Ensure healthy lives and promote well-being for all at all ages
Descripción
Sumario:Charcot-Marie-Tooth disease (CMT) is classified according to neurophysiological and histological findings, the inheritance pattern, and the underlying genetic defect. The objective of these guidelines is to offer recommendations for the diagnosis, prognosis, follow-up, and treatment of this disease in Spain. These consensus guidelines were developed through collaboration by a multidisciplinary panel encompassing a broad group of experts on the subject, including neurologists, paediatric neurologists, geneticists, physiatrists, and orthopaedic surgeons.