Non-syndromic cleft lip and palate: the prevalence of consanguineous parental (2017)
- Authors:
- Autor USP: NEVES, LUCIMARA TEIXEIRA DAS - FOB
- Unidade: FOB
- Subjects: FISSURA LÁBIOPALATINA; PARENTALIDADE
- Language: Inglês
- Abstract: Objective: Cleft lip and palate represent the most common congenital defect and present acomplex etiology involving genetic and environmental factors (Freitas JAS et al, J Appl OralSci, 2011). Environmental factors related to orofacial clefts are associated with maternalhealth and habits during pregnancy (Aquino SN et al, Braz J Otorhinolaryngol, 2011).Regarding genetic/hereditary factors, the issue of familial recurrence and consanguineousmarriages are highlighted. In Brazil, the consanguineous union is heterogeneous and thereare few studies verifying the relationship between it and the occurrence of orofacial clefts(Brito LA et al, American Journal of Medical Genetics, 2011). Thus, the objective of this studywas to verify the prevalence of consanguineous marriages among parents of individuals withnon-syndromic cleft lip and palate. Method and Results: A total of 513 medical records ofindividuals with non-syndromic cleft lip and palate (unilateral or bilateral) were evaluated inthe Hospital for Rehabilitation of Craniofacial Anomalies (HRAC-USP) regardingconsanguineous marriages among parents. Among these, 10 cases of consanguinity werefound between parents. Five cases comprised consanguineous union between first-degreecousins, two cases between 2nd degree cousins, a case between 3rd degree cousins, a casewhere the degree of kinship was not informed and a case between uncle and niece. In thesecases, six were bilateral clefts and four were unilateral. Conclusion: The study revealed aprevalence of 1.94% of consanguineous union among parents of individuals with non-syndromic cleft lip and palate. The most reported was bilateral cleft lip and palate.
- Imprenta:
- Publisher: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo
- Publisher place: Bauru
- Date published: 2017
- Source:
- Título do periódico: Anais
- Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas
-
ABNT
SILVA, Carolina Maia e NEVES, Lucimara Teixeira das. Non-syndromic cleft lip and palate: the prevalence of consanguineous parental. 2017, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2017. Disponível em: https://repositorio.usp.br/directbitstream/d6888e1b-b631-425e-a780-82dc9b3cb3ad/2949022.pdf. Acesso em: 03 jun. 2024. -
APA
Silva, C. M., & Neves, L. T. das. (2017). Non-syndromic cleft lip and palate: the prevalence of consanguineous parental. In Anais. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/d6888e1b-b631-425e-a780-82dc9b3cb3ad/2949022.pdf -
NLM
Silva CM, Neves LT das. Non-syndromic cleft lip and palate: the prevalence of consanguineous parental [Internet]. Anais. 2017 ;[citado 2024 jun. 03 ] Available from: https://repositorio.usp.br/directbitstream/d6888e1b-b631-425e-a780-82dc9b3cb3ad/2949022.pdf -
Vancouver
Silva CM, Neves LT das. Non-syndromic cleft lip and palate: the prevalence of consanguineous parental [Internet]. Anais. 2017 ;[citado 2024 jun. 03 ] Available from: https://repositorio.usp.br/directbitstream/d6888e1b-b631-425e-a780-82dc9b3cb3ad/2949022.pdf - Triagem de mutação no éxon 3 do gene IRF6 em indivíduos com fissura labiopalatina e agenesia dentária: padronização de protocolo para seqüenciamento de DNA genômico a partir de saliva
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 | 2949022.pdf | Direct link |
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