Understanding CHRND Gene Myasthenic Syndrome Congenital Type 3B Fast-Channel Genetic Test CHRND gene myasthenic syndrome congenital type 3B, also known as the fast-channel congenital myasthenic syndrome, is a rare genetic disorder affecting the neuromuscular junction. This condition is characterized by muscle weakness and fatigue, primarily caused by mutations in the CHRND gene. These mutations disrupt […]











