Literature DB >> 11247008

Behavioural and emotional features in Rett syndrome.

R H Mount1, R P Hastings, S Reilly, H Cass, T Charman.   

Abstract

PURPOSE/
METHOD: There is increasing agreement that many genetic disorders have characteristic behavioural phenotypes; that is genetic anomalies have specific effects on behaviour. In this paper the existing literature is reviewed with an aim to identify behavioural and emotional features that are candidates for Rett syndrome (RS) specific behaviours. RESULT/
CONCLUSION: A number of behavioural and emotional features have been reported to be common in individuals with RS. These behaviours may constitute an RS-specific profile of behaviour or behavioural phenotype. Alternatively, these behaviours may simply reflect the multiple disabilities found in individuals with severe or profound cognitive impairment. The diagnostic criteria for Rett syndrome include a number of the behavioural features, such as hand stereotypies and breathing difficulties, although other behavioural features are not included.

Entities:  

Mesh:

Year:  2001        PMID: 11247008     DOI: 10.1080/09638280150504207

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  18 in total

1.  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

2.  MeCP2: only 100% will do.

Authors:  Hsiao-Tuan Chao; Huda Y Zoghbi
Journal:  Nat Neurosci       Date:  2012-01-26       Impact factor: 24.884

3.  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

4.  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

5.  Loss of MeCP2 in cholinergic neurons causes part of RTT-like phenotypes via α7 receptor in hippocampus.

Authors:  Ying Zhang; Shu-Xia Cao; Peng Sun; Hai-Yang He; Ci-Hang Yang; Xiao-Juan Chen; Chen-Jie Shen; Xiao-Dong Wang; Zhong Chen; Darwin K Berg; Shumin Duan; Xiao-Ming Li
Journal:  Cell Res       Date:  2016-04-22       Impact factor: 25.617

Review 6.  Emerging pharmacotherapies for neurodevelopmental disorders.

Authors:  Daniel Z Wetmore; Craig C Garner
Journal:  J Dev Behav Pediatr       Date:  2010-09       Impact factor: 2.225

7.  Sleep-Disordered Breathing in Pediatric Patients With Rett Syndrome.

Authors:  Kathleen M Sarber; Javier J M Howard; Thomas J Dye; John E Pascoe; Narong Simakajornboon
Journal:  J Clin Sleep Med       Date:  2019-10-15       Impact factor: 4.062

8.  Features of autism in Rett syndrome and severe mental retardation.

Authors:  Rebecca H Mount; Tony Charman; Richard P Hastings; Sheena Reilly; Hilary Cass
Journal:  J Autism Dev Disord       Date:  2003-08

Review 9.  The relationship of Rett syndrome and MECP2 disorders to autism.

Authors:  Jeffrey Lorenz Neul
Journal:  Dialogues Clin Neurosci       Date:  2012-09       Impact factor: 5.986

10.  Training communication abilities in Rett Syndrome through reading and writing.

Authors:  Rosa Angela Fabio; Ilaria Castelli; Antonella Marchetti; Alessandro Antonietti
Journal:  Front Psychol       Date:  2013-12-06
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