Long-term follow-up of respiratory function in facioscapulohumeral muscular dystrophy.
Sjan TeeselinkSanne C C VincentenNicol C VoermansJan T GroothuisJonne DoorduinPeter J WijkstraCorinne Gosewina Cornelia HorlingsBaziel G M van EngelenKarlien MulPublished in: Journal of neurology (2022)
Respiratory function remained stable in most patients with FSHD, but a subgroup of patients showed a pronounced deterioration. They showed more severe muscle weakness including the leg muscles at baseline (Ricci score ≥ 6), had spinal and thorax deformities and a relatively fast decline in axial muscle function at follow-up.