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Öğe A CASE OF SECKEL SYNDROME WITH TRICUSPID ATRESIA(MEDECINE ET HYGIENE, 2014) Arslan, D.; Cimen, D.; Guvenc, O.; Sert, A.; Oktay, A.; Oran, B.A case of Seckel syndrome with tricuspid atresia: Seckel syndrome is an autosomal recessive disease presenting with marked growth retardation, microcephalic dwarfism, some facial and skeletal abnormalities. Tricuspid atresia is a rare and life threatening cyanotic congenital heart diseases, with an incidence of 1% to 3%. It is feature of the anatomically normally related great arteries with a large ventricular septum defect and stenosis of right ventricular outflow tract. Tricuspid atresia has never been reported in patients with Seckel syndrome. Here we report a 15-day-old girl baby diagnosed as having Seckel syndrome with tricuspid atresia.Öğe Effects Of High-dose Intravenous Methylprednisolone In Children With Acute Rheumatic Carditis(BLACKWELL SCIENCE, 1996) Akçoral, A.; Oran, B.; Tavlı, V.; Ünal, N.; Çevik, N. T.In order to measure the effects of high-dose intravenous methylprednisolone (HIVMP) and compare its efficiency with that of oral prednisolone (OP), 18 patients with active rheumatic carditis were studied. Ten patients received OF. while eight patients were treated with HIVMP. Clinical and laboratory responses to treatment were followed by sleeping pulse rate, systolic blood pressure, erythrocyte sedimentation rate (ESR), cardiothoracic ratio (CTR), PR interval on electrocardiogram. spectral and color flow imaging and Doppler echocardiographic findings: mitral and aortic regurgitant jet flow area, left atrial area, proximal width of mitral regurgitant jet area and regurgitation fractions. The results of patients in the HIVMP group showed statistically significant changes in SR and CTR when compared with the patients receiving OP, and the recovery was more rapid. HIVMP therapy fan be considered as a new method of treatment for acute rheumatic carditisÖğe Greig cephalopolysyndactyly syndrome: A family report(2010) Alp, H.; Alp, E.; Çimen, Derya; Oran, B.Greig cephalopolysyndactyly syndrome (GCPS) is an autosomal dominant condition characterized by distinct combination of craniofacial, hand and food malformations. It is caused by mutations of the gene GLI3, located on 7p13. The clinical features consistent with GCPS are typical craniofacial findings, post or preaxial polysyndactyly of the hands and feet. In this report we describe clinical and radiological findings of a Turkish family in which five members of three generations could be examined. Dysgenesis of the corpus callosum is diagnosed in one of the patients. A rare clinical manifestation, pectus excavatum, is also seen in two of the cases. Copyright © 2010 by Türkiye Klinikleri.Öğe Hydrocephalus in Mumps Meningoencephalitis - Case-Report(WILLIAMS & WILKINS, 1995) Oran, B.; Çeri, A.; Yılmaz, H.; Kabakuş, N.; Ayçiçek, A.; Erkul, I.[Abstract not Available]Öğe Hydrocephalus in Mumps Meningoencephalitis: Case Report(1995) Oran, B.; Çeri, A.; Yılmaz, H.; Kabakuç, N.; Ayçiçek, A.; Erkul, I.[Abstract not Available]Öğe Oxygen Free Radicals in Children with Acute Rheumatic Fever(GREENWICH MEDICAL MEDIA LTD, 2001) Oran, B.; Atabek, E.; Karaaslan, S.; Reisli, Y.; Gültekin, F.; Erkul, Y.We have investigated the relationship between oxygen free radicals and acute rheumatic fever with regard to diagnosis of the disease process. At the time of diagnosis, we measured the levels of reactive oxygen molecules in the plasma, this being a parameter for oxygen free radicals, and discovered the levels to be significantly higher when compared with those measured in a control group (P<0.05). The levels measured in the plasma, however, were not statistically different among patients with and without carditis. We found a progressive decrease in the levels measured in the plasma when patients with acute rheumatic fever were tested on the 15(th), 30(th) and 90(th) days subsequent to diagnosis. By the 90(th) day, levels measured in the plasma were still higher, but no longer significantly elevated, when compared with the control group. The present study is preliminary, but raises the possibility that measurement of oxygen free radicals in the plasma could be used as a laboratory test for active state of acute rheumatic fever. Further investigations will be needed, nonetheless, to determine the clinical application of this technique.Öğe A Partial Trisomy 15q Due to 15;17 Translocation Detected by Conventional Cytogenetic and Fish Techniques(Medecine Et Hygiene, 2000) Cora, T.; Acar, H.; Oran, B.We report a case having multiple abnormalities including the simultaneous presence of the heart defect and central nerve system abnormalities, which has been reported in a few cases, and with a partial trisomy 15q. Partial trisomy 15q has been inherited from a balanced translocation carried by his phenotypically normal father, detected by traditional banding and fluorescence in situ hybridization (FISH). Application of FISH using whole chromosome specific library probes, locus specific and repetitive probes allowed us to detect the translocation between chromosomes 15q and 17q. Simultaneous application of probes revealed the position of the translocation. interestingly, in addition to the chromosomes 15 pericentromeric signals, the use of chromosome 15 beta-satellite III probe demonstrated an extra signal on chromosome 14 in both metaphase, and lighted three signals interphase nuclei which was inherited from his father. This patient is compared with other partial trisomy 15q patients reported in the literature. The results are also discussed in relation to genetic counselling for the possible relation of chromosome abnormality and clinical findings.Öğe PLASMA LEPTIN, NEUROPEPTIDE Y, GHRELIN AND ADIPONECTIN LEVELS AND CAROTID ARTERY INTIMA MEDIA THICKNESS IN EPILEPTIC CHILDREN TREATED WITH VALPROATE(WILEY-BLACKWELL, 2011) Tokgoz, H.; Aydin, K.; Oran, B.; Kiyici, A.[Abstract not Available]Öğe Plasma levels of soluble osteopontin in children with acute rheumatic fever(WILEY-BLACKWELL, 2008) Unal, E.; Cimen, O.; Oran, B.; Koksal, Y.; Basarili, K.; Baysal, T.; Cimen, D.[Abstract not Available]Öğe Prognostic value of N-terminal pro-B-type natriuretic peptide in children with acute rheumatic carditis: a preliminary report(WILEY-BLACKWELL, 2008) Cimen, O.; Oran, B.; Unal, E.; Basarili, K.; Cimen, D.; Baysal, T.; Buyukbas, S.[Abstract not Available]Öğe Transient Right Sided Hypertrophic Cardiomyopathy in an Infant Born to a Diabetic Mother(1996) Akçoral, A.; Oran, B.; Tavlı, V.; Ören, H.; Çevik, N. T.Hypertrophie cardiomyopathy (HCM) is a rare primary myocardial disease, characterized by hypertrophy of the left and/or right ventricle. Infants of diabetic mothers (IDM) are at risk for development of HCM, respiratory distress and persistent pulmonary hypertension. A case of severe right sided HCM in an infant born to a diabetic mother is presented. The patient's findings were complementary to the previous observations reporting HCM in IDM. The presence of disproportionate septal hypertrophy in the echocardiography of an infant born to a diabetic mother is highly suggestive of HCM in IDM. In our opinion, further cardiac evaluation is not indicated unless other cardiac abnormalities are suspected.
