1. Oral Problems in Brazilian Individuals with Rare Genetic Diseases That Affect Skeletal Development.
- Author
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Rabello F, Celestino MLS, Carneiro NCR, Reis-Oliveira J, Prado HV, Abreu MHNG, and Borges-Oliveira AC
- Subjects
- Humans, Brazil epidemiology, Male, Female, Adult, Cross-Sectional Studies, Child, Child, Preschool, Adolescent, Young Adult, Middle Aged, Prevalence, Mucopolysaccharidoses epidemiology, Mucopolysaccharidoses genetics, Mouth Diseases epidemiology, Malocclusion epidemiology, Dental Caries epidemiology, Osteogenesis Imperfecta epidemiology, Osteogenesis Imperfecta genetics, Rare Diseases epidemiology, Rare Diseases genetics
- Abstract
The present study aimed to compare the prevalence of oral problems between individuals with rare genetic diseases that affect skeletal development and individuals without rare diseases. A cross-sectional study was conducted with 210 individuals between two and fifty-four years of age: 105 with rare genetic diseases (27 with mucopolysaccharidosis [MPS] and 78 with osteogenesis imperfecta [OI]) and 105 without rare diseases. The rare genetic disease group was recruited from hospital units that provide care for patients with MPS and OI in five states of Brazil, and the other group was recruited from the same location. The participants were examined with regards to malocclusion, dental anomalies, dental caries, and gingivitis. A questionnaire was administered addressing individual, sociodemographic, and behavioral characteristics as well as dental history. A descriptive analysis was performed, followed by unadjusted and adjusted binary logistic regression analyses. The mean age was 14.1 ± 12.2 years. Individuals with a rare disease were 12.9-fold more likely to have some type of oral problem (95% CI: 3.7-44.7) compared to the group without rare diseases. The prevalence of oral problems was higher among Brazilians with MPS and OI compared to normotypical individuals.
- Published
- 2024
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