Facioscapulohumeral dystrophy

特許 係属中 Facioscapulohumeral muscular dystrophy (FSHMD, FSHD or FSH), which was originally named Landouzy-Dejerine,[1] is a usually autosomal dominant inherited form of muscular dystrophy (MD)[2] that initially affects the skeletal muscles of the face (facio), scapula (scapulo) and upper arms (humeral). FSHD is widely stated to be the third most common genetic disease of skeletal muscle and Orpha.net lists the prevalence as 4/100,000.