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Öğe Corrected Qt interval in patients with metabolic syndrome(2011) Paksoy, Fatma; Ulaş, Turgay; Bes, Cemal; Dal, Mehmet Sinan; Borlu, FatihObjectives: Metabolic syndrome may be associated with increased cardiovascular mortality and morbidity. However, prolongation of QT intervals due to metabolic syndrome is still unclear. The purpose of this study was to investigate the incidence prolonged QT intervals in pa tients with metabolic syndrome and also demonstrate the relationship between them. Therefore, we aimed to inves tigate the relationship between metabolic syndrome and the QT prolongation in a large patient group. Materials and methods: A total of 1009 individuals were enrolled in this study. Metabolic syndrome was defined according to the IDF criteria and the QTc intervals were measured by using Bazett Formula. QT ≤ 0.44 second was accepted as normal. Results: Totally, 278 male and 731 female individuals of 1009 cases were enrolled in this study. The average dura tion of corrected QT of men according to the Bazzett formula were found as 0,448±0,04 second and QT interval of women were 0,449±0,05 second. QT intervals of both women and men with metabolic syndrome were significantly higher than normal limits of QT interval (p<0,01). Conclusion: Metabolic syndrome found as associated with a prolonged QTc. Results of our study suggest that QTc interval length was increased in patients with metabolic syndrome.Öğe Familial mediterranean fever without cardinal symptoms and role of genetic screening(Page Press Publications, 2012) Ulaş, Turgay; Büyükhatipoğlu, Hakan; Bes, Cemal; Dal, Mehmet Sinan; Hacıbekiroğlu, İlhan; Apucu, Hacı Gökhan; Borlu, FatihFamilial Mediterranean fever is an autosomal recessive disorder characterized by paroxysmal episodes of fever and serosal inflammation. The classical presentation is fever and severe recurrent abdominal pain due to serositis that lasts for one to three days and the resolves spontaneously. Between the episodes patients are asymptomatic. Ninety-five percent of patients with familial mediterranean fever have painful episodes localized to the abdomen, which is usually the dominant manifestation of the disease. Herein, we present a case of a 34-year-old man with incomplete abdominal pain episode of familial mediterranean fever limited to the epigastrum and had no cardinals symptoms of this disease. The diagnosis was made by genetic screening. Successful treatment response was achieved by colchicine.Öğe Primer psoas absesi: Bir olgu sunumu(2012) Ulaş, Turgay; Bes, Cemal; Paksoy, Fatma; Aydoğan, Timuçin; Dal, Mehmet Sinan; Borlu, FatihPsoas absesi nadir görülen, akla getirilmediği sürece güç tanı konabilen bir klinik tablodur. Primer ve sekonder olarak sınıflandırılmaktadır. Sekonder psoas absesi genellikle altta yatan hastalıkların komplikasyonu olarak görülürken, primer psoas absesinin en yaygın etkeni Staphylococcus aureus’tur. Tedavide gecikme artmış morbidite ve mortalite oranları ile ilişkilidir. Bu yazıda, 46 yaşında bel ağrısı nedeniyle başvuran ve manyetik rezonans görüntüleme (MRG) ile psoas kasında abse tespit edilen bir olgu tartışıldı.Öğe Pseudoxanthoma elasticum with mallory-weiss syndrome: Case report(Ortadogu Ad Pres & Publ Co, 2012) Paksoy Türköz, Fatma; Ulaş, Turgay; Beş, Cemal; Özkan, Koray; Sakız, Damlanur; Dal, Mehmet Sinan; Borlu, FatihPseudoxanthoma elasticum is a multi-systemic, genetic disorder of the connective tissue characterized by progressive calcification and fragmentation of elastic fibers in skin, retina, gastrointestinal and cardiovascular systems. Skin changes generally manifest in adulthood and rarely in childhood. Upper gastrointestinal hemorrhage occurs in some cases and is frequently resistant to nonsurgical methods of treatment. As the prognosis of pseudoxanthoma elasticum is related to the involvement of extracutaneous organs, early recognition of the disease is important to take preventive measures and to decrease the morbidity. Herein, we presented a case of pseudoxanthoma elasticum with Mallory-Weiss syndrome, who had repetitive and massive upper gastrointestinal bleeding. To our knowledge, there is no reported case of pseudoxanthoma elasticum with Mallory-Weiss syndrome in the literature.
