Literature DB >> 2344012

Scoliosis in the Rett syndrome: natural history and treatment.

D J Harrison1, P J Webb.   

Abstract

The Rett syndrome (RS) is associated with a neurological form of scoliosis. From 1985 we have instituted a postal survey of families with Rett girls. The prevalence of scoliosis in the survey population is 64%. The age at onset of scoliosis has a normal distribution about a peak age of 8 years, with 72% of cases occurring before age 8. The scoliosis in RS is typically a long thoracolumbar curvature that progresses rapidly in girls over the age of 10 years. Operative treatment is successful in reducing the curvature, preventing curve progression and improving spinal balance for sitting and walking. The 5 girls who walked pre-operatively are still able to do so.

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Year:  1990        PMID: 2344012     DOI: 10.1016/s0387-7604(12)80200-2

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  9 in total

Review 1.  Rett syndrome: a review of current knowledge.

Authors:  R Van Acker
Journal:  J Autism Dev Disord       Date:  1991-12

2.  Rate of complications due to neuromuscular scoliosis spine surgery in a 30-years consecutive series.

Authors:  Francesco Turturro; Antonello Montanaro; Cosma Calderaro; Luca Labianca; Vincenzo Di Sanzo; Andrea Ferretti
Journal:  Eur Spine J       Date:  2017-03-17       Impact factor: 3.134

3.  Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors.

Authors:  John T Killian; Jane B Lane; Hye-Seung Lee; Steve A Skinner; Walter E Kaufmann; Daniel G Glaze; Jeffrey L Neul; Alan K Percy
Journal:  Pediatr Neurol       Date:  2017-02-07       Impact factor: 3.372

4.  Surgical correction of scoliosis in Rett syndrome: cord monitoring and complications.

Authors:  T Hammett; A Harris; B Boreham; S M H Mehdian
Journal:  Eur Spine J       Date:  2014-02-01       Impact factor: 3.134

5.  Intensive Postural and Motor Activity Program Reduces Scoliosis Progression in People with Rett Syndrome.

Authors:  Alberto Romano; Elena Ippolito; Camilla Risoli; Edoardo Malerba; Martina Favetta; Andrea Sancesario; Meir Lotan; Daniel Sender Moran
Journal:  J Clin Med       Date:  2022-01-22       Impact factor: 4.241

6.  Bone mineral content and bone mineral density are lower in older than in younger females with Rett syndrome.

Authors:  Kathleen J Motil; Kenneth J Ellis; Judy O Barrish; Erwin Caeg; Daniel G Glaze
Journal:  Pediatr Res       Date:  2008-10       Impact factor: 3.756

7.  Mecp2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndrome.

Authors:  R D O'Connor; M Zayzafoon; M C Farach-Carson; N C Schanen
Journal:  Bone       Date:  2009-05-03       Impact factor: 4.398

8.  Long-term follow-up of functioning after spinal surgery in patients with Rett syndrome.

Authors:  Eva-Lena Larsson; Stig Aaro; Peter Ahlinder; Helena Normelli; Hans Tropp; Birgitta Oberg
Journal:  Eur Spine J       Date:  2009-01-23       Impact factor: 3.134

9.  Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with bone disease severity in Rett syndrome.

Authors:  Carla Caffarelli; Stefano Gonnelli; Maria Dea Tomai Pitinca; Silvia Camarri; Antonella Al Refaie; Joussef Hayek; Ranuccio Nuti
Journal:  BMC Med Genet       Date:  2020-01-31       Impact factor: 2.103

  9 in total

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