Access to oral health care services for individuals with rare genetic diseases affecting skeletal development

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dc.creatorSuélen Alves Teixeira Debossan
dc.creatorTahyná Duda Deps
dc.creatorHeloisa Vieira Prado
dc.creatorMauro Henrique Nogueira Guimarães Abreu
dc.creatorAna Cristina Borges de Oliveira
dc.date.accessioned2025-03-10T16:02:04Z
dc.date.accessioned2025-09-09T00:43:02Z
dc.date.available2025-03-10T16:02:04Z
dc.date.issued2022
dc.description.sponsorshipCNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico
dc.description.sponsorshipFAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais
dc.description.sponsorshipCAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
dc.identifier.doihttps://doi.org/10.1111/scd.12639
dc.identifier.issn1754-4505
dc.identifier.urihttps://hdl.handle.net/1843/80569
dc.languagepor
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofSpecial Care in Dentistry
dc.rightsAcesso Restrito
dc.subjectHealth services accessibility
dc.subjectRare diseases
dc.subjectMouth diseases
dc.subjectHealth of the disabled
dc.subject.otherDental care for the disabled
dc.subject.otherHealth service accessibility
dc.subject.otherMucopolysaccharidoses
dc.subject.otherOsteogenesis imperfecta
dc.subject.otherRare genetic diseases
dc.titleAccess to oral health care services for individuals with rare genetic diseases affecting skeletal development
dc.typeArtigo de periódico
local.citation.epage40
local.citation.spage32
local.citation.volume42
local.description.resumoObjective: To identify factors associated with oral health care services for indi-viduals with and without rare genetic diseases.Materials and Method: A cross-sectional study was undertaken, with 140 indi-viduals paired by sex and age (70 with rare genetic diseases and 70 without), agedbetween 3 and 27 years, and their parents. The sample was selected from two ref-erence hospitals for patients with rare genetic diseases in southeastern Brazil.The parents completed a questionnaire on individual aspects and their child’smedical/dental history. Participants who did and did not suffer from rare geneticdiseases were examined for dental caries, malocclusion, dental anomalies, andoral hygiene. The theoretical model Directed Acyclic Graphs (DAG) was used toidentify possible confounding variables in the association between rare diseasesand access to dental care. Descriptive analyses and non-matched and matchedlogistic regression models (p < 0.05) were carried out.Results: The chance of individuals without rare genetic disease having accessto oral health care service was 5.32 times higher (95% CI 2.35–12.01) than thosewith such conditions. Individuals who had not suffered upper respiratory tractinfections had a 3.16 times greater chance of being in the group with access tooral health care service (95% CI 1.45–6.90).Conclusion: Individuals with no rare genetic diseases and no history of upperrespiratory tract infections had a greater chance of belonging to the group of indi-viduals with access to a dental service. Individuals with rare genetic diseases haveless access to oral health care.
local.identifier.orcidhttps://orcid.org/0000-0002-1529-9311
local.publisher.countryBrasil
local.publisher.departmentFAO - DEPARTAMENTO DE ODONTOLOGIA SOCIAL E PREVENTIVA
local.publisher.initialsUFMG
local.url.externahttps://onlinelibrary.wiley.com/doi/epdf/10.1111/scd.12639

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