👉 Geoffroy's disease is a rare genetic disorder characterized by severe muscular weakness, often affecting the face, arms, and legs. It is caused by mutations in the gene encoding for the protein called myosin light chain (MLC). This mutation typically occurs during embryonic development and can lead to muscle atrophy, causing a loss of strength and coordination. The disease affects approximately 1 in every 20,000 individuals worldwide, with a high prevalence in Europe and North America
Geoffroy's