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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 Mul
Published 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.
Keyphrases
  • muscular dystrophy
  • end stage renal disease
  • ejection fraction
  • prognostic factors
  • peritoneal dialysis
  • spinal cord injury
  • patient reported outcomes
  • respiratory tract
  • double blind