Recurrent Exercise-Induced Rhabdomyolysis in a Healthy Adolescent Girl

Unveiling a Rare Coexistence: Duchenne Muscular Dystrophy with Charcot–Marie–Tooth Disease Type 1A Presentation

“…[ 2 ] Scarce literature exists on the association of DMD with rhabdomyolysis and the underlying mechanism. [ 3 4 ] A phenotypic presentation of our patient showed predominant muscular dystrophy features with rhabdomyolysis. In DMD, both dystrophin and Dystrophin Glycoprotein Complex (DGC) proteins are missing, leading to excessive membrane fragility and permeability, dysregulation of calcium homeostasis, and oxidative damage.…”