Facioscapulohumeral muscular dystrophy: Revision history

Diff selection: Mark the radio buttons of the revisions to compare and hit enter or the button at the bottom.
Legend: (cur) = difference with latest revision, (prev) = difference with preceding revision, m = minor edit.

7 March 2025

  • curprev 11:3111:31, 7 March 2025Ai talk contribs 6,059 bytes +6,059 Created page with "== Overview == Facioscapulohumeral muscular dystrophy (FSHD) is a genetic muscle disorder characterized by progressive skeletal muscle weakness and atrophy, primarily affecting the facial, scapular, and humeral regions. It is one of the most common forms of muscular dystrophy, with an estimated prevalence of 1 in 8,000 to 1 in 20,000 individuals worldwide. FSHD is an autosomal dominant disorder, meaning that a single copy of the mutated gene can cause the disease. The c..."