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ÖZTÜRK ÖZENER, HAFİZE

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ÖZTÜRK ÖZENER

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HAFİZE

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2017 - 201912020 - 20221
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    PublicationOpen Access
    Single nucleotide polymorphisms in IL-1A RS1800587, IL-1B RS1143634 and vitamin D receptor rs731236 in stage III grade B/C periodontitis
    (2022-06-01) ÖZTÜRK ÖZENER, HAFİZE; ASLAN, BEGÜM; AĞRALI, ÖMER BİRKAN; ULUCAN, KORKUT; YILDIRIM, HATİCE SELİN; KURU, LEYLA; Ozener H., ASLAN B., Eken B. F., AĞRALI Ö. B., Yildrim H. S., Altunok E. C., ULUCAN K., KURU L.
    The purpose of the study is to determine the prevalence of interleukin (IL)-1A (rs1800587), IL-1B (rs1143634) and vitamin D receptor (VDR) (TaqI, rs731236) gene polymorphisms in the Turkish population and their association with Stage III Grade B/C periodontitis. Systemically and periodontally healthy individuals (N = 100) and Stage III Grade B/C periodontitis patients (N=100) based on clinical and radiographic examination were included in this research. Clinical attachment level, probing depth, bleeding on probing, plaque and gingival indices of the subjects were measured. Genotyping of IL-1A (rs1800587), IL-1B (rs1143634) and VDR (rs731236) polymorphisms was conducted by Real Time PCR. Allelic and genotypic distributions of IL-1A (rs1800587) gene polymorphism were not associated with periodontitis (p > 0.05). In IL-1B (rs1143634) gene polymorphism, the C allele was detected more frequently in healthy individuals compared with the periodontitis patients (p=0.045). CC genotype and C allele in VDR (rs731236) gene polymorphism was higher in periodontitis patients (p=0.031, p=0.034, respectively). In comparison with Grade B periodontitis patients and healthy subjects, CC genotype and C allele were observed more frequently in the Grade B periodontitis in terms of alleles (C/T) and genotypes for VDR (rs731236) polymorphism (p=0.024, p=0.008, respectively). This study presents that the VDR (rs731236) polymorphism are associated with enhanced susceptibility to Stage III periodontitis in the Turkish population. Furthermore, VDR (rs731236) polymorphism may be used as an identification criteria to discriminate Grade B and Grade C in Stage III periodontitis.
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    Multidisciplinary Therapy in a Patient with Amelogenesis Imperfecta: A Case Report With 5-Year Follow-Up
    (AVES PRESS LTD, 2017) ÖZTÜRK ÖZENER, HAFİZE; Ozener, Hafize Ozturk; Gemalmaz, Deniz; Kuru, Bahar
    Amelogenesis imperfecta (AI) is a hereditary disorder that disrupts the formation of dental enamel in the primary and permanent dentition in the absence of systemic manifestations. The main concerns are caries susceptibility, poor esthetics, and generalized sensitivity. Treating these defects is not only important for esthetics and function but also for psychosocial health. Treatment planning for patients with AI is related to many factors: age and socioeconomic status of the patient, type and severity of the disorder, and the intraoral situation. In this case report, the 5-year results of a periodontal leveling process and fixed prosthetic restoration performed to regain esthetic and functional requirements in a female patient diagnosed with hypomature AI are presented.