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The Rett Syndrome behaviour questionnaire (RSBQ): refining the behavioural and emotional phenotype of Rett syndrome

The Rett Syndrome behaviour questionnaire (RSBQ): refining the behavioural and emotional phenotype of Rett syndrome
The Rett Syndrome behaviour questionnaire (RSBQ): refining the behavioural and emotional phenotype of Rett syndrome
Although physical features, including loss of hand skills, deceleration of head growth, spasticity and scoliosis, are cardinal features of Rett syndrome (RS), a number of behavioural features are also associated with the disorder, including hand stereotypies, hyperventilation and breath holding. No study has tested the specificity of these behavioural features to individuals with RS, compared to individuals with severe to profound mental retardation (SMR). Method:
A novel checklist of characteristic RS behavioural and emotional features, the Rett Syndrome Behaviour Questionnaire (RSBQ), was developed to test the type and specificity of behavioural features of RS against those found in girls with SMR. Results:
After controlling for the effects of RS-related physical disabilities, the RSBQ discriminated between the groups. Some aspects of the behaviours found to be specific to RS are included in the necessary or supportive RS diagnostic criteria, notably hand behaviours and breathing problems. Additional behavioural features were also more frequently reported in the RS than the SMR group, including mood fluctuations and signs of fear/anxiety, inconsolable crying and screaming at night, and repetitive mouth and tongue movements and grimacing. Conclusions:
Full validation of the scale requires confirmation of its discriminatory power and reliability with independent samples of individuals with RS and SMR. Further delineation of the specific profile of behaviours seen in RS may help in identification of the function of the MECP2 gene and in improved differential diagnosis and management of individuals with RS.
Rett syndrome, behavioural phenotype, mental retardation, MECP2, diagnosis, questionnaire
0021-9630
1099-1110
Mount, R.H.
078c66e2-7408-44f9-8f37-afaf00742ad0
Charman, T.
6acd5100-63cf-4e5a-94c0-f1b9f039d32c
Hastings, R.P.
7c2e6f17-c5e8-47bc-baff-137dd6ce9f9a
Reilly, S.
44ecaf59-36fb-4d3c-bb83-de6d4d4e3894
Cass, H.
d3dc500d-ee14-4f79-a153-47d4dfa926c4
Mount, R.H.
078c66e2-7408-44f9-8f37-afaf00742ad0
Charman, T.
6acd5100-63cf-4e5a-94c0-f1b9f039d32c
Hastings, R.P.
7c2e6f17-c5e8-47bc-baff-137dd6ce9f9a
Reilly, S.
44ecaf59-36fb-4d3c-bb83-de6d4d4e3894
Cass, H.
d3dc500d-ee14-4f79-a153-47d4dfa926c4

Mount, R.H., Charman, T., Hastings, R.P., Reilly, S. and Cass, H. (2002) The Rett Syndrome behaviour questionnaire (RSBQ): refining the behavioural and emotional phenotype of Rett syndrome. Journal of Child Psychology and Psychiatry, 43 (8), 1099-1110. (doi:10.1111/1469-7610.00236).

Record type: Article

Abstract

Although physical features, including loss of hand skills, deceleration of head growth, spasticity and scoliosis, are cardinal features of Rett syndrome (RS), a number of behavioural features are also associated with the disorder, including hand stereotypies, hyperventilation and breath holding. No study has tested the specificity of these behavioural features to individuals with RS, compared to individuals with severe to profound mental retardation (SMR). Method:
A novel checklist of characteristic RS behavioural and emotional features, the Rett Syndrome Behaviour Questionnaire (RSBQ), was developed to test the type and specificity of behavioural features of RS against those found in girls with SMR. Results:
After controlling for the effects of RS-related physical disabilities, the RSBQ discriminated between the groups. Some aspects of the behaviours found to be specific to RS are included in the necessary or supportive RS diagnostic criteria, notably hand behaviours and breathing problems. Additional behavioural features were also more frequently reported in the RS than the SMR group, including mood fluctuations and signs of fear/anxiety, inconsolable crying and screaming at night, and repetitive mouth and tongue movements and grimacing. Conclusions:
Full validation of the scale requires confirmation of its discriminatory power and reliability with independent samples of individuals with RS and SMR. Further delineation of the specific profile of behaviours seen in RS may help in identification of the function of the MECP2 gene and in improved differential diagnosis and management of individuals with RS.

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More information

Published date: 2002
Keywords: Rett syndrome, behavioural phenotype, mental retardation, MECP2, diagnosis, questionnaire

Identifiers

Local EPrints ID: 57720
URI: http://eprints.soton.ac.uk/id/eprint/57720
ISSN: 0021-9630
PURE UUID: f49c0f46-2229-4a9b-9c63-c488827e1464

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Date deposited: 11 Aug 2008
Last modified: 15 Mar 2024 11:08

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Contributors

Author: R.H. Mount
Author: T. Charman
Author: R.P. Hastings
Author: S. Reilly
Author: H. Cass

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