Literature DB >> 26373460

Ageing in Rett syndrome.

R Cianfaglione1, A Clarke2, M Kerr1, R P Hastings3, C Oliver4, D Felce1.   

Abstract

BACKGROUND: The aim was to gain a UK national sample of people with Rett syndrome across the age range and (1) conduct a cross-sectional comparison of age groups and (2) undertake a longitudinal follow-up.
METHODS: From 308 potential participants approached to take part, a sample of 91 girls and women was achieved (29.5%). Their ages ranged from 4 to 47 years, and 71 were known to have a mutation in the methyl-CpG binding protein-2 (MECP2) gene. Seventy-two of the initial sample were followed up 16 months later, and 50 returned completed assessments (69.4%). Their ages ranged from 7 to 48 years, and 42 were MECP2 positive. Parental questionnaire measures of Rett syndrome specific characteristics, impulsivity, overactivity, mood, interest and pleasure, repetitive behaviour and self-injury were administered.
RESULTS: Adaptive behaviour and behavioural characteristics of Rett syndrome were similar across age groups and, where assessed, stable over time, as were repetitive behaviours generally and self-injury. There was some suggestion of deterioration in health arising with ageing, principally contributed to by deteriorations in dental and gastro-intestinal problems both with moderate effect sizes. Indicators of mood, interest and pleasure differed significantly across age groups. The total scale score significantly deteriorated over time, with a moderate effect size.
CONCLUSIONS: This study provides further evidence for the post-regression stability that characterises Rett syndrome. Emergent low mood in Rett syndrome requires further research.
© 2015 MENCAP and International Association of the Scientific Study of Intellectual and Developmental Disabilities and John Wiley & Sons Ltd.

Entities:  

Keywords:  Rett syndrome; ageing; intellectual disabilities

Mesh:

Year:  2015        PMID: 26373460     DOI: 10.1111/jir.12228

Source DB:  PubMed          Journal:  J Intellect Disabil Res        ISSN: 0964-2633


  7 in total

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2.  Caregiver- and Clinician-Reported Adaptive Functioning in Rett Syndrome: a Systematic Review and Evaluation of Measurement Strategies.

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Journal:  Neuropsychol Rev       Date:  2019-11-20       Impact factor: 7.444

3.  Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndrome.

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Journal:  Neurology       Date:  2019-03-27       Impact factor: 9.910

4.  Sex disparate gut microbiome and metabolome perturbations precede disease progression in a mouse model of Rett syndrome.

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5.  Challenges in the Dental Management of Rett Syndrome under General Anesthesia: A Rare Disease.

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6.  The behavioural phenotype of SATB2-associated syndrome: a within-group and cross-syndrome analysis.

Authors:  Stacey Bissell; Chris Oliver; Joanna Moss; Mary Heald; Jane Waite; Hayley Crawford; Vishakha Kothari; Lauren Rumbellow; Grace Walters; Caroline Richards
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7.  Phenotypes in adult patients with Rett syndrome: results of a 13-year experience and insights into healthcare transition.

Authors:  Angela Peron; Maria Paola Canevini; Filippo Ghelma; Rosangela Arancio; Miriam Nella Savini; Aglaia Vignoli
Journal:  J Med Genet       Date:  2020-10-26       Impact factor: 6.318

  7 in total

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