Browsing by Author "Yilmaz, Aysegul"
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Premature ovarian failure due to tetrasomy X in an adolescent girl
Kara, Cengiz; Utyol, Ala; Yilmaz, Aysegul; Altundag, Engin; Ogur, Gonul (Springer, 2014)Tetrasomy X associated with premature ovarian failure has been described in a few patients, and the parental origin of the extra X chromosomes has not been investigated so far in this group. A 15-year-old girl with mental ... -
A Retrospective Evaluation of the Patients with Congenital Heart Disease in Neonatal Intensive Care Unit
Erturk, Emine Yurdakul; Kucukoduk, Sukru; Baysal, Kemal; Ayyildiz, Pelin; Yilmaz, Aysegul; Ogur, Gonul (Galenos Yayincilik, 2016)Introduction: Congenital heart disease (CHD) is the most common congenital anomaly in newborns. In this study it was aimed to investigate the demographic features of the patients with CHD diagnosed in neonatal intensive ... -
A Skeptical Approach to the Management of Persistent Oral Ulceration in a Child
Kartal, Ibrahim; Dagdemir, Ayhan; Elli, Murat; Yildiz, Levent; Yilmaz, Aysegul (Hindawi Ltd, 2018)The diagnosis of oral lesions is sometimes difficult due to both the clinician's limited experience with the conditions that may cause the lesions and their similar appearances, especially in children. Correctly establishing ... -
Vesicourethral Reflux-Induced Renal Failure in a Patient with ICF Syndrome Due to a Novel DNMT3B Mutation
Kutlug, Seyhan; Ogur, Gonul; Yilmaz, Aysegul; Thijssen, Peter E.; Abur, Ummet; Yildiran, Alisan (Wiley, 2016)ICF syndrome is a primary immunodeficiency disease characterized by hypo-or agammaglobulinemia, centromeric instability mainly on chromosomes 1, 9, and 16 and facial anomalies. ICF syndrome presents with frequent respiratory ...
