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Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Treatment of Symptoms in Children with Q3 Conditions Scoping Review Results
Text
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URL Address
<a href="http://doi.org/10.1002/ajmg.a.37502" target="_blank" rel="noreferrer noopener">http://doi.org/10.1002/ajmg.a.37502</a>
Dublin Core
The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.
Title
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Sleep disturbance in Mowat-Wilson syndrome
Publisher
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American Journal of Medical Genetics Part A
Date
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2016
Subject
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Middle Aged; Male; Severity of Illness Index; Surveys and Questionnaires; Child; Humans; Adult; Adolescent; Female; Child Preschool; Australia; Mutation; Facies; Hirschsprung Disease/di [Diagnosis]; Intellectual Disability/di [Diagnosis]; Microcephaly/di [Diagnosis]; Sleep Initiation and Maintenance Disorders/di [Diagnosis]; 0 (Homeodomain Proteins); 0 (Repressor Proteins); 0 (ZEB2 protein human); Behavior Rating Scale; Gene Expression; Hirschsprung Disease/co [Complications]; Hirschsprung Disease/ge [Genetics]; Hirschsprung Disease/pp [Physiopathology]; Homeodomain Proteins/ge [Genetics]; Intellectual Disability/co [Complications]; Intellectual Disability/ge [Genetics]; Intellectual Disability/pp [Physiopathology]; Microcephaly/co [Complications]; Microcephaly/ge [Genetics]; Microcephaly/pp [Physiopathology]; Mowat-Wilson syndrome; Repressor Proteins/ge [Genetics]; Sleep Initiation and Maintenance Disorders/co [Complications]; Sleep Initiation and Maintenance Disorders/ge [Genetics]; Sleep Initiation and Maintenance Disorders/pp [Physiopathology]; sleep disturbance/disorders; Mowat-Wilson syndrome; trajectory; characteristics
Creator
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Evans E; Mowat D; Wilson M; Einfeld S
Description
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Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly syndrome caused by a heterozygous mutation or deletion of the ZEB2 gene. It is characterized by a distinctive facial appearance in association with intellectual disability (ID) and variable other features including agenesis of the corpus callosum, seizures, congenital heart defects, microcephaly, short stature, hypotonia, and Hirschsprung disease. The current study investigated sleep disturbance in people with MWS. In a series of unstructured interviews focused on development and behaviors in MWS, family members frequently reported sleep disturbance, particularly early-morning waking and frequent night waking. The Sleep Disturbance Scale for Children (SDSC) was therefore administered to a sample of 35 individuals with MWS, along with the Developmental Behaviour Checklist (DBC) to measure behavioral and emotional disturbance. A high level of sleep disturbance was found in the MWS sample, with 53% scoring in the borderline range and 44% in the clinical disorder range for at least one subscale of the SDSC. Scores were highest for the Sleep-wake transition disorders subscale, with 91% of participants reaching at least the borderline disorder range. A significant positive association was found between total scores on the SDSC and the DBC Total Behaviour Problem Score. These results suggest that sleep disorders should be screened for in people with MWS, and where appropriate, referrals to sleep specialists made for management of sleep problems.Copyright © 2015 Wiley Periodicals, Inc.
Identifier
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<a href="http://doi.org/10.1002/ajmg.a.37502" target="_blank" rel="noreferrer noopener">10.1002/ajmg.a.37502</a>
Rights
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Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
0 (Homeodomain Proteins)
0 (Repressor Proteins)
0 (ZEB2 protein human)
2016
Adolescent
Adult
American Journal of Medical Genetics Part A
Australia
Behavior Rating Scale
characteristics
Child
Child Preschool
Einfeld S
Evans E
Facies
Female
Gene Expression
Hirschsprung Disease/co [Complications]
Hirschsprung Disease/di [Diagnosis]
Hirschsprung Disease/ge [Genetics]
Hirschsprung Disease/pp [Physiopathology]
Homeodomain Proteins/ge [Genetics]
Humans
Intellectual Disability/co [Complications]
Intellectual Disability/di [Diagnosis]
Intellectual Disability/ge [Genetics]
Intellectual Disability/pp [Physiopathology]
Male
Microcephaly/co [Complications]
Microcephaly/di [Diagnosis]
Microcephaly/ge [Genetics]
Microcephaly/pp [Physiopathology]
Middle Aged
Mowat D
Mowat-Wilson syndrome
Mutation
Repressor Proteins/ge [Genetics]
Severity Of Illness Index
sleep disturbance/disorders
Sleep Initiation and Maintenance Disorders/co [Complications]
Sleep Initiation and Maintenance Disorders/di [Diagnosis]
Sleep Initiation and Maintenance Disorders/ge [Genetics]
Sleep Initiation and Maintenance Disorders/pp [Physiopathology]
Surveys And Questionnaires
Trajectory
Wilson M