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Updated: Jun 24, 2026

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Murine Fetal Echocardiography
Published on: February 15, 2013
Ultrasound structural fetal anomaly screening: an update
1Fetal Medicine, Rosie Maternity, Addenbrookes Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Archives of Disease in Childhood. Fetal and Neonatal Edition
|March 25, 2009
Summary
Routine ultrasound screening for fetal anomalies is common in the UK, but methods vary. This review covers common structural anomalies detected at 11-14 and 18-23 week scans, exploring new diagnostic techniques.
Area of Science:
- Medical Imaging
- Prenatal Diagnosis
- Obstetrics
Background:
- Ultrasound screening for fetal anomalies became routine in UK maternity units by the late 1970s.
- Congenital abnormalities affect up to 5% of newborns.
- Current screening practices lack uniformity in timing and methodology.
Purpose of the Study:
- To review current knowledge on screening for common structural fetal anomalies.
- To discuss advancements in ultrasound techniques for improved screening accuracy.
- To focus on anomalies detected during the 11-14 and 18-23 week scans.
Main Methods:
- Literature review of existing studies on fetal anomaly screening.
- Analysis of established ultrasound protocols for specific gestational ages.
- Exploration of emerging technologies in prenatal imaging.
Main Results:
- Significant progress has been made in identifying structural fetal anomalies via ultrasound.
- New techniques show promise for enhancing screening accuracy and diagnostic capabilities.
- Variability in current screening practices necessitates standardization.
Conclusions:
- Ultrasound remains a cornerstone for detecting structural fetal anomalies.
- Continued research and technological innovation are crucial for optimizing prenatal screening.
- Standardized approaches to ultrasound screening can improve detection rates and patient outcomes.
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