Literature DB >> 23347273

Early development and regression in Rett syndrome.

J Y L Lee1, H Leonard, J P Piek, J Downs.   

Abstract

This study utilized developmental profiling to examine symptoms in 14 girls with genetically confirmed Rett syndrome and whose families were participating in the Australian Rett syndrome or InterRett database. Regression was mostly characterized by loss of hand and/or communication skills (13/14) except one girl demonstrated slowing of skill development. Social withdrawal and inconsolable crying often developed simultaneously (9/14), with social withdrawal for shorter duration than inconsolable crying. Previously acquired gross motor skills declined in just over half of the sample (8/14), mostly observed as a loss of balance. Early abnormalities such as vomiting and strabismus were also seen. Our findings provide additional insight into the early clinical profile of Rett syndrome.
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  MECP2; Rett syndrome; autistic symptoms; development; regression

Mesh:

Year:  2013        PMID: 23347273     DOI: 10.1111/cge.12110

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  11 in total

Review 1.  Rett syndrome and MeCP2.

Authors:  Vichithra R B Liyanage; Mojgan Rastegar
Journal:  Neuromolecular Med       Date:  2014-03-11       Impact factor: 3.843

2.  Co-occurrence of Dystonic and Dyskinetic Tongue Movements with Oral Apraxia in Post-regression Dysphagia in Classical Rett Syndrome Years of Life 1 Through 5.

Authors:  Suzanne S Abraham; Ben Taragin; Alesandra Djukic
Journal:  Dysphagia       Date:  2014-12-23       Impact factor: 3.438

Review 3.  Clinical and biological progress over 50 years in Rett syndrome.

Authors:  Helen Leonard; Stuart Cobb; Jenny Downs
Journal:  Nat Rev Neurol       Date:  2016-12-09       Impact factor: 42.937

4.  Repeated Motor Training on Attention Reaching Skills and Stereotypies in Rett Syndrome.

Authors:  Rosa Angela Fabio; Samantha Giannatiempo; Tindara Caprì; Martina Semino
Journal:  Mov Disord Clin Pract       Date:  2022-05-19

Review 5.  Quantitative and qualitative insights into the experiences of children with Rett syndrome and their families.

Authors:  Jenny Downs; Helen Leonard
Journal:  Wien Med Wochenschr       Date:  2016-08-04

6.  The trajectories of sleep disturbances in Rett syndrome.

Authors:  Kingsley Wong; Helen Leonard; Peter Jacoby; Carolyn Ellaway; Jenny Downs
Journal:  J Sleep Res       Date:  2014-09-14       Impact factor: 3.981

7.  Early development in Rett syndrome - the benefits and difficulties of a birth cohort approach.

Authors:  Peter B Marschik; Sanne Lemcke; Christa Einspieler; Dajie Zhang; Sven Bölte; Gillian S Townend; Marlene B Lauritsen
Journal:  Dev Neurorehabil       Date:  2017-05-23       Impact factor: 2.308

8.  Hand stereotypies: Lessons from the Rett Syndrome Natural History Study.

Authors:  Jennifer L Stallworth; Marisela E Dy; Caroline B Buchanan; Chin-Fu Chen; Alexandra E Scott; Daniel G Glaze; Jane B Lane; David N Lieberman; Lindsay M Oberman; Steven A Skinner; Aubin E Tierney; Gary R Cutter; Alan K Percy; Jeffrey L Neul; Walter E Kaufmann
Journal:  Neurology       Date:  2019-05-03       Impact factor: 9.910

9.  Three different profiles: early socio-communicative capacities in typical Rett syndrome, the preserved speech variant and normal development.

Authors:  Peter B Marschik; Katrin D Bartl-Pokorny; Helen Tager-Flusberg; Walter E Kaufmann; Florian Pokorny; Tobias Grossmann; Christian Windpassinger; Erwin Petek; Christa Einspieler
Journal:  Dev Neurorehabil       Date:  2013-10-02       Impact factor: 2.308

10.  Eye Gaze Technology as a Form of Augmentative and Alternative Communication for Individuals with Rett Syndrome: Experiences of Families in The Netherlands.

Authors:  Gillian S Townend; Peter B Marschik; Eric Smeets; Raymond van de Berg; Mariёlle van den Berg; Leopold M G Curfs
Journal:  J Dev Phys Disabil       Date:  2015-10-19
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