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Updated: Jan 28, 2026

Fetal Echocardiography and Pulsed-wave Doppler Ultrasound in a Rabbit Model of Intrauterine Growth Restriction
Published on: June 29, 2013
Neonatal Morbidities of Fetal Growth Restriction: Pathophysiology and Impact
Atul Malhotra1,2,3, Beth J Allison2,4, Margie Castillo-Melendez2,4
1Monash Newborn, Monash Children's Hospital, Melbourne, VIC, Australia.
Insights
Fetal growth restriction (FGR) causes babies to be born small, leading to health issues. Understanding FGR
Area of Science:
- Obstetrics and Gynecology
- Neonatology
- Developmental Biology
Background:
- Intrauterine growth restriction (FGR) is a pregnancy complication characterized by pathological fetal growth reduction.
- Placental insufficiency is the primary cause, leading to chronic undersupply of oxygen and nutrients to the fetus.
- Neonatal morbidities depend on FGR onset, severity, and gestational age at birth.
Purpose of the Study:
- To explore pathophysiological mechanisms of major neonatal morbidities in FGR.
- To examine the impact of FGR on infant health.
- To present clinical, diagnostic, and management strategies for neonatal morbidities.
Main Methods:
- Review of pathophysiological mechanisms in FGR.
- Analysis of fetal cardiovascular adaptation and organ development.
- Compilation of clinical presentation, diagnostic tools, and management strategies.
Main Results:
- Fetal cardiovascular adaptation and altered organ development are key contributors to postnatal consequences.
- Neonatal morbidities vary based on FGR timing, severity, and gestational age.
- Current targeted therapies and their status are discussed.
Conclusions:
- Understanding FGR's pathophysiological mechanisms is crucial for neonatal health.
- Early detection, monitoring, and management of adverse outcomes are essential.
- Improved knowledge facilitates better care for newborns affected by FGR.
Abstract:
Being born small lays the foundation for short-term and long-term implications for life. Intrauterine or fetal growth restriction describes the pregnancy complication of pathological reduced fetal growth, leading to significant perinatal mortality and morbidity, and subsequent long-term deficits. Placental insufficiency is the principal cause of FGR, which in turn underlies a chronic undersupply of oxygen and nutrients to the fetus. The neonatal morbidities associated with FGR depend on the timing of onset of placental dysfunction and growth restriction, its severity, and the gestation at birth of the infant. In this review, we explore the pathophysiological mechanisms involved in the development of major neonatal morbidities in FGR, and their impact on the health of the infant. Fetal cardiovascular adaptation and altered organ development during gestation are principal contributors to postnatal consequences of FGR. Clinical presentation, diagnostic tools and management strategies of neonatal morbidities are presented. We also present information on the current status of targeted therapies. A better understanding of neonatal morbidities associated with FGR will enable early neonatal detection, monitoring and management of potential adverse outcomes in the newborn period and beyond.
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