Effective monitoring of fetal growth is a key aspect of antenatal care. The
short-term complications of fetal growth restriction (FGR) include stillbi
rth, prematurity, perinatal morbidity and decreased fetal reserve during la
bour. At the other end of the spectrum, macrosomia is associated with birth
trauma and neonatal metabolic disturbances. Evidence also exists that thes
e growth disturbances may have long-term complications for several organ sy
stems extending well beyond childhood [1]. Therefore, any advance in the su
rveillance and prevention of deranged fetal growth is likely to reap large
social and economic benefits.
The clinical performance of screening methods for FGR remains poor. Screeni
ng policies for detecting the small for-gestational age (SGA) baby using cl
inical methods succeed in only approximately a quarter of cases [2,3]. It h
as also been questioned whether, with current methods, antenatal detection
actually improves outcome [4]. A systematic review of randomized trials sug
gests that, to date, most prenatal interventions do not show any significan
t effects on Short-term perinatal outcome [5].
In this article we focus on recent developments in our understanding of fet
al growth abnormalities and their clinical detection.