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[Significant association between nonsyndromic cleft lip with or without cleft palate and IRF6rs2235371 polymorphism in Iranian familiar population].
Jafary, F; Nadeali, Z; Salehi, M; Hosseinzadeh, M; Sedghi, M; Gholamrezapour, T; Nouri, N.
Afiliação
  • Jafary F; Pediatric Inherited Disease Research Center (PIDRC), Isfahan University of Medical Sciences, Isfahan, Iran.
  • Nadeali Z; Young Researchers and Elite Club, Falavarjan Branch, Islamic Azad University, Isfahan, Iran.
  • Salehi M; Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Hosseinzadeh M; Department of Genetics and Molecular Biology, Medical School, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Sedghi M; Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
  • Gholamrezapour T; Pediatric Inherited Disease Research Center (PIDRC), Isfahan University of Medical Sciences, Isfahan, Iran.
  • Nouri N; Medical Genetics Laboratory, Alzahra University Hospital, Isfahan University of Medical Sciences, Isfahan, Iran.
Mol Biol (Mosk) ; 49(6): 949-52, 2015.
Article em Ru | MEDLINE | ID: mdl-26710774
ABSTRACT
According to previous studies the IRF6rs2235371 polymorphism is a risk factor for NSCL/P in different populations. However our recent study revealed no correlation between IRF6rs642961 and NSCL/P in our population. In the present study we have investigated the relationship between IRF6rs2235371 and NSCL/P in same group to determine whether IRF6rs2235371 is a risk factor in our population as well. We analyzed the IRF6rs2235371 genotype in a subset of the Iranian population using the Polymerase Chain Reaction technique. The PCR products were digested with DpnII. Chi-square test was applied to analyze the obtained result. The patients were supplied by the Cleft Lip and Palate Clinic of the Isfahan University of Medical Science. A clinician ascertained the non-syndromic status of all patients and that no clefting drugs, ethanol or smoking were abused during pregnancy. The control group was selected from unaffected subjects with no history of NSCL/P in their families. 107 patients from 107 Iranian unrelated families and 100 controls were screened. There was a significant association between the IRF6rs2235371 genotype sand an increased NSCL/P risk. Our data indicates that the IRF6rs2235371 variation can increase the risk of NSCL/P in the Iranian population. This result is in contrast with the results of our recent study on the correlation between the IRF6rs642961 polymorphism and NSCL/P in the same group.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenda Labial / Fissura Palatina / Polimorfismo de Nucleotídeo Único / Fatores Reguladores de Interferon Tipo de estudo: Observational_studies Limite: Humans País/Região como assunto: Asia Idioma: Ru Revista: Mol Biol (Mosk) Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Irã

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenda Labial / Fissura Palatina / Polimorfismo de Nucleotídeo Único / Fatores Reguladores de Interferon Tipo de estudo: Observational_studies Limite: Humans País/Região como assunto: Asia Idioma: Ru Revista: Mol Biol (Mosk) Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Irã