2019-04-14, OTCU H., YAKUT K., UZUNER S., USTABAŞ KAHRAMAN F., ERENBERK U., YOZGAT Y., OTÇU TEMUR, HAFİZE, UZUNER, SELÇUK, USTABAŞ KAHRAMAN, FEYZA, ERENBERK, UFUK, YOZGAT, YILMAZ

2018-04-11T00:00:00Z, Yozgat, Yılmaz, Çakır, Erkan, Otçu Temur, Hafize, Yakut, Kahraman, Yazan, Hakan, Erenberk, Ufuk, Uzuner, Selçuk, YOZGAT, YILMAZ, ÇAKIR, ERKAN, OTÇU TEMUR, HAFİZE, YAKUT, KAHRAMAN, YAZAN, HAKAN, ERENBERK, UFUK, UZUNER, SELÇUK

2020-12-01T00:00:00Z, Yozgat, Can Yilmaz, UZUNER, SELÇUK, OTÇU TEMUR, Hafize, ERGÖR, Serap Nur, GULİYEVA, AYNUR, Tahaoglu, Irmak, Coban, Senay, YOZGAT, YILMAZ, UZUNER, SELÇUK, OTÇU TEMUR, HAFİZE, ERGÖR, SERAP NUR, GULİYEVA, AYNUR, YOZGAT, YILMAZ

Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) accounts for 0.023% of all cases reported in pediatric patients. According to literature, only a handful of ALCAPA patients are able to reach adulthood. Clinical manifestations of ALCAPA range from fatigue during exercise to sudden death in adulthood. Herein, we described a 12-year-old symptomatic patient with ALCAPA who had severe chest pain after using salbutamol treatment for presumed asthma. ALCAPA is one of the curable versions of myocardial ischemia and infarction in childhood. Due to clinical findings in conjunction with electrocardiogram and echocardiography, a computed tomography scan with coronary angiography was performed and the diagnosis of ALCAPA was confirmed. We presented this case because ALCAPA-related myocardial ischemia and infarction in children are rare with only sporadic cases reported. This case illustrated the need for close monitoring and surgery as the best treatment for ALCAPA associated with myocardial infarction.

2019-04-14, YAKUT K., OTCU H., UZUNER S., USTABAŞ KAHRAMAN F., ERENBERK U., YOZGAT Y., OTÇU TEMUR, HAFİZE, UZUNER, SELÇUK, USTABAŞ KAHRAMAN, FEYZA, ERENBERK, UFUK, YOZGAT, YILMAZ

2020-07-01T00:00:00Z, Yozgat, Can Yilmaz, YEŞİLBAŞ, Osman, UZUNER, SELÇUK, SARITAŞ, BETÜL, ERGÖR, Serap Nur, OTÇU TEMUR, Hafize, YOZGAT, Yılmaz, YEŞİLBAŞ, OSMAN, UZUNER, SELÇUK, SARITAŞ, BETÜL, ERGÖR, SERAP NUR, OTÇU TEMUR, HAFİZE, YOZGAT, YILMAZ

2020-09-01T00:00:00Z, OTÇU TEMUR, Hafize, Yozgat, Can Yilmaz, UZUNER, SELÇUK, Ugurlucan, Murat, YAZAN, HAKAN, ÇAKIR, Erkan, YOZGAT, Yılmaz, OTÇU TEMUR, HAFİZE, UZUNER, SELÇUK, YAZAN, HAKAN, ÇAKIR, ERKAN, YOZGAT, YILMAZ

Double aortic arch (DAA) is a common form of complete vascular ring. The state of the condition leads to upper airway impediment and compression of the esophagus. A balanced DAA is an extremely rare anomaly. The anatomical aberration cannot be easily diagnosed with echocardiography when an infant has chronic respiratory distress. Herein, we present the case of an 11-month-old girl who had chronic respiratory distress and a balanced DAA.

2018-04-21, YOZGAT Y., YAKUT K., OTCU H., ERENBERK U., UZUNER S., USTABAŞ KAHRAMAN F., YOZGAT, YILMAZ, OTÇU TEMUR, HAFİZE, ERENBERK, UFUK, UZUNER, SELÇUK, USTABAŞ KAHRAMAN, FEYZA

2018-04-12T00:00:00Z, Gulieva, Aynur, Yozgat, Yılmaz, Çakır, Erkan, Otçu Temur, Hafize, Erenberk, Ufuk, Uzuner, Selçuk, Al Shadfan, Lina Muhammed, Yakut, Kahraman, YOZGAT, YILMAZ, ÇAKIR, ERKAN, OTÇU TEMUR, HAFİZE, ERENBERK, UFUK, UZUNER, SELÇUK, YAKUT, KAHRAMAN