Person: BAYRAKTAR, BILGE
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Kurumdan Ayrılmıştır
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BILGE
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BAYRAKTAR
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Publication Metadata only Comparasion of two different doses of sucrose in pain relief by using Bernese Pain Scale for neonates(2016-11-01) TANYERİ, BİLGE; BAYRAKTAR, BILGEPublication Metadata only A new case series of Crisponi syndrome in a Turkish family and review of the literature(2017-04-01) TANYERİ, BİLGE; BAYRAKTAR, BILGEPublication Metadata only Intraocular pressure in infants and its association with hormonal changes with vaginal birth versus cesarean section.(2016-12-01) Elbay, AHMET; CELIK, U; CELIK, BURAK; OZER, OF; KILIC, GÖKHAN; AKKAN, JC; BAYRAKTAR, BİLGE; KAYMAK, NZ; ELBAY, AHMET; ÇELİK, BURAK; ÖZER, ÖMER FARUK; KILIC, GÖKHAN; BAYRAKTAR, BILGEPublication Metadata only The relation of urinary bisphenol A with kisspeptin in girls diagnosed with central precocious puberty and premature thelarche.(2016-03-01T00:00:00Z) Ozgen, Ilker Tolga; Torun, EMEL; Bayraktar-Tanyeri, Bilge; Durmaz, Erdem; Kilic, Elif; Cesur, Yasar; ÖZGEN, İLKER TOLGA; TORUN, EMEL; BAYRAKTAR, BILGE; CESUR, YAŞARBackground: Bisphenol A (BPA) is known as an endocrine disruptor and it is supposed to have a role on the development of central precocious puberty (CPP). Kisspeptin, a hypothalamic peptide, is a neuromodulator of gonadotropin releasing hormone and it has an important role on regulation of the onset of puberty. The BPA levels in girls with CPP and premature thelarche (PT) and its relation with kisspeptin levels were investigated.Publication Metadata only Freeman-Sheldon Syndrome Associated with Hemophilia-A in a Newborn(2016-12-01T00:00:00Z) BAYRAKTAR, Bilge; Bayraktar, Suleyman; ARSLAN, HÜSEYİN; ÇAKIR, FATMA BETÜL; BAYRAKTAR, BILGE; ÇAKIR, FATMA BETÜLThe Freeman-Sheldon syndrome (FSS) (whistling face) is a congenital autosomal dominant disease (rarely described in its autosomal recessive form) characterized by small -whistling- mouth, a flat masklike face, joint contractures (commonly involving the fingers and hands) and underdevelopment of the nasal cartilage. Other clinical features include full forehead, deep set eyes, epicanthal folds, high palate, H-shaped cutaneous dimpling on the chin, ulnar deviation of the hands, seizures, and dislocation of the hip. A 10-day-old male newborn was admitted to our neonatal intensive care unit with jaundice and hyperthermia. He had fever of 42.5 degrees C, small whistling mouth, a flat mask-like face, joint contractures of the fingers, and ulnar deviation of the hands. The parents were consanguineous and one of the boys died when he was 1 years old due to intracranial hemorrhage. To our knowledge, there have been more than 60 cases diagnosed with FSS. This is the first reported case of Freeman-Sheldon syndrome associated with hemophilia A and the second case of FSS associated with fever without anesthesia.Publication Open Access Infantile Pompe Disease Presenting with Severe Hypertrophic Cardiomyopathy: A Case Report(2015-09-01T00:00:00Z) Bayraktar, Suleyman; BAYRAKTAR, Bilge; Elevli, Murat; BAYRAKTAR, BILGEInfantile Pompe disease (glycogen storage disease type 2) is a fatal disease with autosomal recessive inheritance, leading to hypertrophic cardiomyopathy, hypotonia and respiratory failure. It is a progressive condition due to accumulation of glycogen in the muscles. We aimed to present a case of infantile Pompe disease in a patient who had giant QRS complexes in electrocardiographic monitoring and hypertrophic cardiomyopathy involving the interventricular septum and the left ventricle on echocardiography.