Disease | scoliosis |
Phenotype | C0026850|muscular dystrophy |
Sentences | 9 |
PubMedID- 23752144 | Methods: vital capacity (vc), peak cough flow, and the extent of ventilator dependence were documented before and after surgical correction of scoliosis for children with duchenne muscular dystrophy (dmd) and spinal muscular atrophy (sma) with vcs as low as 2%. |
PubMedID- 20358328 | This study was performed to determine the efficacy and safety of stopping segmental pedicle screw constructs at l5 during surgical treatment of scoliosis associated with duchenne muscular dystrophy (dmd). |
PubMedID- 24599203 | Conclusions: surgery in patients who had duchenne muscular dystrophy with scoliosis improved function and decreased the rate of deterioration of forced vital capacity compared with patients treated conservatively. |
PubMedID- 24986949 | We report the incidence of and risk factors for complications after scoliosis surgery in patients with duchenne muscular dystrophy (dmd) and compare them with those of other neuromuscular conditions. |
PubMedID- 23450561 | Background: scoliosis in people with duchenne muscular dystrophy is usually progressive and treated with surgery. |
PubMedID- 23560735 | Non-surgical prevention and management of scoliosis for children with duchenne muscular dystrophy: what is the evidence. |
PubMedID- 19533124 | Autogenous iliac crest bone graft versus banked allograft bone in scoliosis surgery in patients with duchenne muscular dystrophy. |
PubMedID- 23783200 | Glucocorticoid treatment for the prevention of scoliosis in children with duchenne muscular dystrophy: long-term follow-up. |
PubMedID- 26423318 | Background: scoliosis in patients with duchenne muscular dystrophy (dmd) is usually progressive and is treated with surgery. |
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