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
2014,
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;