Abstract Background There is relatively little literature on the oral health experiences of individuals with Rett syndrome. This study described the incidence of dental extractions and restorations in a population-based cohort, according to a range of demographic and clinical factors. The association between bruxism and age was also investigated. Methods Existing questionnaire data in the population-based Australian Rett Syndrome Database for the years 2004, 2006, 2009 or 2011 on genetically confirmed female cases (n = 242) were analysed. Results The incidence rate of restorations and extractions were 6.8 per 100 person years (py) and 9.3 per 100 py respectively. The incidence of extractions decreased with increasing levels of income. Compa...
Background: Rett Syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized ...
Population-based longitudinal observational study.To describe the prevalence of scoliosis in Rett sy...
There is often delay between onset of Rett syndrome symptoms and its diagnosis, possibly related to ...
Objectives: Rett syndrome (RS) is a rare disease with oral manifestations that have not been describ...
Rett syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developme...
Rett syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developme...
PubMed ID: 10204460Rett syndrome is a unique and puzzling disorder noted in females and is possibly ...
Oral health in a group of patients with Rett syndrome in the regions of Valencia and Murcia (Spain):...
Rett syndrome (RS) is a neurological disease that occurs onlyin females and it manifests with mental...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
Background: The aim was to gain a UK national sample of people with Rett syndrome across the age ran...
BackgroundAlthough it is known that patients with primary Sjögren's syndrome (pSS) have impaired den...
STUDY DESIGN.: Population-based longitudinal observational study. OBJECTIVES.: To describe the preva...
Modifications to diagnostic criteria and introduction of genetic testing have likely affected the pa...
Background: Rett Syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized ...
Population-based longitudinal observational study.To describe the prevalence of scoliosis in Rett sy...
There is often delay between onset of Rett syndrome symptoms and its diagnosis, possibly related to ...
Objectives: Rett syndrome (RS) is a rare disease with oral manifestations that have not been describ...
Rett syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developme...
Rett syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developme...
PubMed ID: 10204460Rett syndrome is a unique and puzzling disorder noted in females and is possibly ...
Oral health in a group of patients with Rett syndrome in the regions of Valencia and Murcia (Spain):...
Rett syndrome (RS) is a neurological disease that occurs onlyin females and it manifests with mental...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
As part of a wider study to investigate the behavioral phenotype of a national sample of girls and w...
Background: The aim was to gain a UK national sample of people with Rett syndrome across the age ran...
BackgroundAlthough it is known that patients with primary Sjögren's syndrome (pSS) have impaired den...
STUDY DESIGN.: Population-based longitudinal observational study. OBJECTIVES.: To describe the preva...
Modifications to diagnostic criteria and introduction of genetic testing have likely affected the pa...
Background: Rett Syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized ...
Population-based longitudinal observational study.To describe the prevalence of scoliosis in Rett sy...
There is often delay between onset of Rett syndrome symptoms and its diagnosis, possibly related to ...