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Updated: Jun 7, 2025

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High Frequency Ultrasound for the Analysis of Fetal and Placental Development In Vivo
Published on: November 8, 2018
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Untreated ALCAPA diagnosed in gestational ultrasonography
Lam Truong Hoai1, Nguyen Van Thanh2, Nguyen Cong Thanh2
1Cardiovascular Department, Tam Anh Hospital, Hanoi, Viet Nam.
Radiology Case Reports
|November 19, 2024
Summary
Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital heart defect. This case highlights a pregnant patient with ALCAPA, emphasizing early diagnosis and monitoring during pregnancy.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Cardiovascular Imaging
Background:
- Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly with high mortality if untreated.
- Untreated ALCAPA poses significant risks during pregnancy, including maternal and fetal mortality.
- Congenital heart disease screening is crucial for early diagnosis and management in women of reproductive age.

