Congenital Anomalies: Early Screening & Intervention

Early detection and intervention of congenital anomalies are critical to improving outcomes in affected infants. This session explores the latest advances in prenatal screening, diagnostic imaging, and postnatal management of structural and functional anomalies. Topics include congenital heart defects, neural tube defects, cleft lip/palate, and gastrointestinal malformations. Presentations will highlight the role of genetic testing, ultrasound markers, and fetal echocardiography in early identification. The session also covers multidisciplinary approaches to prenatal counseling, surgical planning, and coordinated delivery. Experts will discuss postnatal treatment options and long-term outcomes based on early detection. Attendees will learn best practices for integrating screening protocols into maternal and newborn care. Designed for pediatricians, neonatologists, obstetricians, and geneticists, this session provides a platform to discuss innovative solutions for addressing congenital anomalies and ensuring timely, effective care from diagnosis through postnatal life.

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