Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Sleep problems in Rett syndrome.

Brain & development - 1 Nov 2007

Young Deidra, Nagarajan Lakshmi, de Klerk Nick, Jacoby Peter, Ellaway Carolyn, Leonard Helen

Abstract excerpt

Rett syndrome (RTT) is a severe neurological disorder, affecting mainly females. It is generally caused by mutations in the MECP2 gene. Sleep problems are thought to occur commonly in Rett syndrome, but there has been little research on prevalence or natural history. An Australian population-based registry of cases born since 1976 has been operating since 1993, with current ascertainment at 300. The Australian...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Surveys and Questionnaires
Share to Age Factors
Share to Australia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Linear Models

Share to Methyl-CpG-Binding Protein 2

Share to Rett Syndrome

Share to Sleep Wake Disorders

Source

Open in PubMed Open full text

Identifiers

PMID: 17531413
DOI: 10.1016/j.braindev.2007.04.001
PMCID: PMC2527512

Genes

MECP2
ARSD

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Sleep problems in Rett syndrome.PMID 17531413Read ↗

Determinants of sleep disturbances in Rett syndrome: Novel findings in relation to genotype.Semantic proximity Read ↗

The trajectories of sleep disturbances in Rett syndrome.Semantic proximity Read ↗

Associations between genotype, phenotype and behaviours measured by the Rett syndrome behaviour questionnaire in Rett syndrome.Semantic proximity Read ↗

Seizures in Rett syndrome: an overview from a one-year calendar study.Semantic proximity Read ↗

Epilepsy and the natural history of Rett syndrome.Semantic proximity Read ↗

Phenotypes in adult patients with Rett syndrome: results of a 13-year experience and insights into healthcare transition.Semantic proximity Read ↗

Rett syndrome: revised diagnostic criteria and nomenclature.Semantic proximity Read ↗

Genetic and clinical variations in a Norwegian sample diagnosed with Rett syndrome.Semantic proximity Read ↗

Genotype and sleep independently predict mental health in Rett syndrome: an observational study.Semantic proximity Read ↗

Describing the phenotype in Rett syndrome using a population database.Semantic proximity Read ↗

Epilepsy in Rett syndrome: association between phenotype and genotype, and implications for practice.Semantic proximity Read ↗

Epilepsy in classic Rett syndrome: Course and characteristics in adult age.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.