Case Report
Complex Congenital Cardiac Anomalies and Complex Tapvc-A Case Report
Vasudha N1*, Pramod N2 and Jeetendra P3
1Department of Anatomy, University Kasaba Bawada, India
2Department of Radiodiagnosis, D.Y.Patil Medical College, India
3Department of Radiodiagnosis, D.Y. Patil Medical College, India
*Corresponding author: Vasudha N, Professor Department of Anatomy, D. Y. Patil Medical College, DY Patil Education Society; Deemed to be University Kasaba Bawada, Kolhapur, Tel: 9665730990; E-mail: dr.vasudhanikam@gmail.com
Copyright: © 2019 Vasudha N, et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Article Information: Submission: 07/05/2019; Accepted: 19/09/2019; Published: 23/09/2019
Abstract
Complex cardiac anomalies are the main cause of infant mortality. Early diagnosis and proper mode of treatment is essential in these cases. Screening of
the patients detects the significant congenital heart defects. We present a case of complex cardiac anomalies with Atrial Septal Defect (ASD), Total Anomalous
Pulmonary Venous Connection (TAPVC), dilated right atrial and right ventricular chambers, Patent Ductus Arteriosus (PDA), Persistent Left Sided Superior
Vena Cava (PLSVC).
