Arikan, SanemOzturk, OnurAtalay, AyferAtalay, Erol Omer2026-06-192026-06-1920261661-65961422-0067https://doi.org/10.3390/ijms27020923https://hdl.handle.net/20.500.12899/5201Beh & ccedil;et's disease is a chronic, multisystem inflammatory disorder characterized by recurrent mucocutaneous and ocular manifestations, in which genetic factors, particularly cytokine gene polymorphisms, are thought to contribute to disease susceptibility. This study aimed to investigate the association of Interleukin-12B and Interleukin-23R gene polymorphisms and haplotype distributions with Beh & ccedil;et's disease in Denizli, a province of Turkey. A total of 88 patients with Beh & ccedil;et's disease and 133 healthy controls were genotyped for Interleukin-12B (rs3213119, rs3213120, rs3212227, rs3213113, rs2082412) and Interleukin-23R (rs1004819, rs7517847, rs7530511, rs10489629, rs10889677) polymorphisms using polymerase chain reaction-restriction fragment length polymorphism analysis. Genotype, allele, and haplotype distributions were evaluated for associations with Beh & ccedil;et's disease risk and clinical manifestations. The results demonstrated that the Interleukin-12B rs2082412 G allele and rs3213119 G allele were associated with increased risk of Beh & ccedil;et's disease. Additionally, the Interleukin-23R rs7530511 TT genotype and rs10489629 GG genotype and G allele were significantly associated with Beh & ccedil;et's disease susceptibility. Haplotype analyses revealed AAAGG and GTCAC as the most frequent haplotypes in Interleukin-12B and Interleukin-23R loci, respectively, in both patients and controls. These findings suggest that Interleukin-12B and Interleukin-23R gene polymorphisms and haplotypes may be associated with Beh & ccedil;et's disease susceptibility and clinical heterogeneity in this population.eninfo:eu-repo/semantics/openAccessBeh & Ccedil;Et'S DiseaseInterleukin-12BInterleukin-23RHaplotypeSingle Nucleotide PolymorphismArticle10.3390/ijms27020923272415965682-s2.0-105028711834Q1WOS:001670609300001Q10000-0003-3404-4135