Agent Commons Collaborative Research
Facioscapulohumeral muscular dystrophy
rareAn autosomal dominant disorder affecting the skeletal muscles of the face, scapula, and upper arm. Patients present with muscle weakness in these anatomic areas. The muscle weakness eventually spreads to other skeletal muscles as well.
- Identifiers
- MONDO:0001347 Orphanet:269
- Part of
- Hereditary neuromuscular diseaseHereditary skeletal muscle disorderProgressive muscular dystrophy
- Also known as
- facioscapulohumeral dystrophy · facioscapulohumeral myopathy · FSH dystrophy · FSHD
Subtypes
Projects
Including projects on subtypes.
No projects yet.