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

Oral parafunction and bruxism in Rett syndrome and associated factors: An observational study.

Oral diseases - 1 Jan 2023

Lai Yvonne Yee Lok, Downs Jenny Anne, Wong Kingsley, Zafar Sobia, Walsh Laurence James, Leonard Helen Margaret

Abstract excerpt

OBJECTIVES: To explore patterns of parafunction, and bruxism, and its relationships with genotype and snoring in individuals with Rett syndrome (RTT). METHODS: Retrospective observational data of those with confirmed MECP2 mutations in the InterRett database (n = 216) were used to investigate experience of parafunctional habits, and bruxism and their relationships with genotype and snoring using multivariable...

Read the complete abstract on PubMed

Topics

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

Share to Genotype
Share to Mutation
Share to Rett Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 34033206
DOI: 10.1111/odi.13924

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Oral parafunction and bruxism in Rett syndrome and associated factors: An observational study.PMID 34033206Read ↗

Sleep problems in Rett syndrome.Semantic proximity Read ↗

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

Genetic Polymorphisms in ACTN3 Contribute to the Etiology of Bruxism in Children.Semantic proximity Read ↗

Epigenetics and Bruxism: Possible Role of Epigenetics in the Etiology of Bruxism.Semantic proximity Read ↗

Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome.Semantic proximity Read ↗

Using wearables to investigate and understand breathing irregularities in Rett syndrome in Australian population-based and Italian clinic samplesSemantic proximity Read ↗

Polymorphic variants in genes related to stress coping are associated with the awake bruxism.Semantic proximity Read ↗

Associations Among Diurnal Salivary Cortisol Patterns, Medication Use, and Behavioral Phenotype Features in a Community Sample of Rett Syndrome.Semantic proximity Read ↗

Genetic polymorphisms and bruxism: A scoping review.Semantic proximity Read ↗

Single nucleotide polymorphisms in dopamine receptor D2 are associated with bruxism and its circadian phenotypes in children.Semantic proximity Read ↗

Genetic analysis of probable sleep bruxism and its associations with clinical and behavioral traits.Semantic proximity Read ↗

People with MECP2 mutation-positive Rett disorder who converse.Semantic proximity Read ↗

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