Charcot-Marie-Tooth disease is a group of genetic diseases that cause damage to the peripheral nerves (nerves that connect the spinal cord to muscles and sensory organs) of the arms and legs (neuropathy). It is also known as hereditary motor and sensory neuropathy (HMSN).
Common symptoms are muscle weakness and wasting in the legs (feet and calves) and later in the hands and forearms; Balance problems and sensory symptoms in the hands and feet. Onset usually occurs during childhood or young adulthood with symptoms such as walking difficulties (stumbling, falling, etc.), a decrease in manual dexterity and foot deformities.
This document, published to coincide with the AFM-Téléthon General Meeting 2024, presents myotonic dystrophy type 2 research news from the past year (ongoing studies and clinical trials, scientific and medical publications, etc.).
Access the document Advances in Charcot-Marie-Tooth disease – June 2024
