Literature DB >> 9452912

The prevalence and incidence of Rett syndrome in Australia.

H Leonard1, C Bower, D English.   

Abstract

The Australian Paediatric Surveillance Unit and the Rett Syndrome Association of Australia (a parent support group) were the main sources of ascertainment of cases of Rett syndrome (RS) aged 18 years or less in Australia. Further information was obtained from questionnaires to paediatricians and families. Cases were categorised as classical, atypical, potential or non-verifiable, using internationally recognised criteria. Capture recapture methods were used to adjust prevalence measures for missing cases, and Kaplan Meier survival analysis to estimate cumulative incidence. A total of 134 cases of RS was identified, and of those over 5 years of age, 68% were classical and 32% were atypical. The adjusted prevalence was 0.72 per 10,000 females, and the cumulative incidence was 0.96 per 10,000 females to age 12 years. The prevalence was similar to that in Sweden and Scotland, but higher than in Texas. Comparing successive birth cohorts, there was evidence to suggest that RS is being diagnosed earlier and that more cases are being diagnosed as atypical.

Entities:  

Mesh:

Year:  1997        PMID: 9452912

Source DB:  PubMed          Journal:  Eur Child Adolesc Psychiatry        ISSN: 1018-8827            Impact factor:   4.785


  30 in total

1.  Evaluation of a national surveillance unit.

Authors:  M Gazarian; K Williams; E Elliott; K Chant; H Longbottom; C Mellis; T Nolan; R K Oates; A Ruben
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2.  The role of prenatal, obstetric and neonatal factors in the development of autism.

Authors:  Linda Dodds; Deshayne B Fell; Sarah Shea; B Anthony Armson; Alexander C Allen; Susan Bryson
Journal:  J Autism Dev Disord       Date:  2011-07

3.  Describing the phenotype in Rett syndrome using a population database.

Authors:  L Colvin; S Fyfe; S Leonard; T Schiavello; C Ellaway; N De Klerk; J Christodoulou; M Msall; H Leonard
Journal:  Arch Dis Child       Date:  2003-01       Impact factor: 3.791

4.  The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders.

Authors:  Daniel C Tarquinio; Wei Hou; Jeffrey L Neul; Walter E Kaufmann; Daniel G Glaze; Kathleen J Motil; Steven A Skinner; Hye-Seung Lee; Alan K Percy
Journal:  Pediatr Neurol       Date:  2015-06-26       Impact factor: 3.372

Review 5.  Rett syndrome: clinical review and genetic update.

Authors:  L S Weaving; C J Ellaway; J Gécz; J Christodoulou
Journal:  J Med Genet       Date:  2005-01       Impact factor: 6.318

6.  The association between behavior and genotype in Rett syndrome using the Australian Rett Syndrome Database.

Authors:  Laila Robertson; Sonĵa E Hall; Peter Jacoby; Carolyn Ellaway; Nick de Klerk; Helen Leonard
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2006-03-05       Impact factor: 3.568

7.  Development of a video-based evaluation tool in Rett syndrome.

Authors:  S Fyfe; J Downs; O McIlroy; B Burford; J Lister; S Reilly; C L Laurvick; C Philippe; M Msall; W E Kaufmann; C Ellaway; H Leonard
Journal:  J Autism Dev Disord       Date:  2006-12-16

8.  Clinical severity and quality of life in children and adolescents with Rett syndrome.

Authors:  J B Lane; H-S Lee; L W Smith; P Cheng; A K Percy; D G Glaze; J L Neul; K J Motil; J O Barrish; S A Skinner; F Annese; L McNair; J Graham; O Khwaja; K Barnes; J P Krischer
Journal:  Neurology       Date:  2011-10-19       Impact factor: 9.910

9.  Rare disease surveillance: An international perspective.

Authors:  E J Elliott; A Nicoll; R Lynn; V Marchessault; R Hirasing; G Ridley
Journal:  Paediatr Child Health       Date:  2001-05       Impact factor: 2.253

10.  Prolonged QT interval in Rett syndrome.

Authors:  C J Ellaway; G Sholler; H Leonard; J Christodoulou
Journal:  Arch Dis Child       Date:  1999-05       Impact factor: 3.791

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