Titre : | Advances in Charcot-Marie-Tooth disease : Avancées dans la maladie de Charcot-Marie-Tooth |
Revue : | Avancées de la recherche |
Auteurs : | Myoinfo, Auteur ; Attarian S, Validateur ; Vallat JM, Validateur ; Gilby E, Auteur |
Type de document : | Publication AFM |
Editeur : | AFM-TELETHON, 06/2022 |
Collection : | Savoir & Comprendre |
Pages : | 35 p |
Langues: | Anglais |
Mots-clés : | diagnostic ; essai clinique ; maladie de Charcot-Marie-Tooth ; physiopathologie ; thérapie génique |
Résumé : |
Charcot-Marie-Tooth (CMT) disease is a group of clinically and genetically heterogeneous diseases, characterised by damage to the peripheral nerves of the upper and lower limbs.
This damage mainly causes muscle weakness, hand and foot sensory disorders (and at times, pain) and balance disorders. Most of the time, the condition begins in childhood or young adulthood, with walking difficulties or foot deformities. This document, published to coincide with the AFM-Téléthon General Meeting 2022, presents news from the past year about research on Charcot-Marie-Tooth disease (international symposia, ongoing clinical trials or studies, scientific and medical publications, etc.). > CMT > Hereditary motor and sensory neuropathies (HMSN) > Hereditary motor neuropathies (HMN) > Charcot-Marie-Tooth neuropathies > Dejerine-Sottas disease |
Lien associé : | Page dédiée à la maladie Charcot-Maire-Tooth sur le site AFM-TELETHON |
Voir aussi : |
Documents numériques (1)
AV22_CMT_not79709_eng.pdf Adobe Acrobat PDF |