Alcapa Syndrome In An Asymptomatic Newborn With Dilated Cardiomyopathy

ABDULLAH ALPINAR, HAYRULLAH ALP, SEVİM KARAARSLAN, TAMER BAYSAL

  • Yıl : 2014
  • Cilt : 30
  • Sayı : Ek
  •  Sayfa : 46-48
Anomalous left coronary artery from pulmonary artery (ALCAPA) is a rare congenital heart disease in which left coronary artery leaves from the pulmonary artery. Patients are usually asymptomatic in neonatal period during the pulmonary artery pressure decreases up to a critical level. However, afterwards left ventricular failure and infarction were present. An asymptomatic newborn patient who was referred our clinic due to cardiac murmur was presented. Dilated cardiomyopathy and anomalous left coronary artery from pulmonary artery were diagnosed with echocardiography and during the cardiac catheterization ALCAPA syndrome was confirmed.
Atıf yapmak için :
Açıklama : Yazarların hiçbiri, bu makalede bahsedilen herhangi bir ürün, aygıt veya ilaç ile ilgili maddi çıkar ilişkisine sahip değildir. Araştırma, herhangi bir dış organizasyon tarafından desteklenmedi.Yazarlar çalışmanın birincil verilerine tam erişim izni vermek ve derginin talep ettiği takdirde verileri incelemesine izin vermeyi kabul etmektedirler.
Alcapa Syndrome In An Asymptomatic Newborn With Dilated Cardiomyopathy
, Vol. 30 (Ek)
Geliş Tarihi : 21.05.2013, Kabul Tarihi : 21.05.2013, Yayın Tarihi : 13.08.2018
Selçuk Tıp Dergisi
ISSN:1017-6616;
E-ISSN:2149-8059;