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OTÇU TEMUR, HAFİZE

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HAFİZE
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OTÇU TEMUR
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Now showing 1 - 3 of 3
  • PublicationMetadata only
    kısa dönem azitromisin profilaksisi alan kronik akciğer hastalıklı çocuk hastalarda qtc süresinde uzama
    (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
  • PublicationOpen Access
    A Rare Cause of Pulmonary Hypertension in a 4-Year-Old Toddler: Association of Cor Triatriatum Sinister and Pulmonary Arteriovenous Malformation
    (2020-11-01T00:00:00Z) Yozgat, Can Yilmaz; ÇAKIR, Erkan; YAZAN, HAKAN; OTÇU TEMUR, Hafize; YAKUT, KAHRAMAN; YOZGAT, YILMAZ; ÇAKIR, ERKAN; YAZAN, HAKAN; OTÇU TEMUR, HAFİZE; YAKUT, KAHRAMAN; YOZGAT, YILMAZ
    Cor triatriatum sinister is a rare congenital cardiac anomaly. The anomaly is caused by a fibromuscular membrane that divides the left atrium into two cavities. This membrane can lead to the obstruction of left atrial flow and also create pulmonary venous hypertension. Pulmonary arteriovenous malformation (PAVM) is notorious for its aberrant blood flow between the pulmonary arteries and veins. Herein, we report a case of a 4-year-old toddler who had a unique form of pulmonary hypertension presenting with cor triatriatum sinister and diffuse PAVM. After the surgical treatment of cor triatriatum sinister, both pulmonary arteriovenous malformation and pulmonary hypertension disappeared.
  • PublicationMetadata only
    Balanced Double Aortic Arch Causing Persistent Respiratory Symptoms Mimicking Asthma in an Infant
    (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.