Inflammation-induced fibrosis in skeletal muscle of female carriers of Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is an X-chromosomal recessively inherited disease, which affects boys from early childhood on. Loss or severe reduction of dystrophin protein induces a plethora of different physiological mechanisms finally leading to myofibre necrosis, atrophy, structural abnormalities, loss of homeostatic functions, and exhaustion of satellite cells. Over time, skeletal and cardiac muscles undergo structural remodelling with development of fibrosis and fatty tissue replacement.
Source: Neuromuscular Disorders - Category: Neurology Authors: Corinna Preu ße, Arpad von Moers, Heike Kölbel, Debora Pehl, Hans-Hilmar Goebel, Ulrike Schara, Werner Stenzel Source Type: research
More News: Boys | Brain | Child Development | Muscular Dystrophy | Neurology | Reflex Sympathetic Dystrophy