RT - Journal Article T1 - A case report of variant scimitar syndrome JF - babol-cjp YR - 2017 JO - babol-cjp VO - 3 IS - 2 UR - http://caspianjp.ir/article-1-71-en.html SP - 253 EP - 256 K1 - Scimitar Syndrome K1 - Pulmonary venous K1 - Congenital Abnormality K1 - Right lung hypoplasia K1 - Coarctation aorta AB - Background: Scimitar syndrome (SS) or congenital pulmonary venolobar syndrome is a rare anomaly, most commonly including partial pulmonary venous drainage into the inferior vena cava, right lung hypoplasia, dextroposition of the heart, and anomalous systemic arterial supply from aorta or one of its branches to the right lung. Case report: A 10-day-old female infant was referred to our hospital with systolic murmur and tachypnea. Initial chest x-ray suggested cardiomegaly and displacement of cardiac structures into the right hemithorax, and initial echocardiogram indicated patent ductus arteriosus, coarctation of aorta, atrial septal defect, ventricular septal defect in this infant who was diagnosed as having SS. Conclusions: We can consider Scimitar syndrome for infants with tachypnea, cyanosis, intrauterine growth restriction (IUGR) and right lobe opacity in chest x-ray. LA eng UL http://caspianjp.ir/article-1-71-en.html M3 10.22088/acadpub.BUMS.3.2.253 ER -