ABSTRACT:One of the major factors affecting nephrogenesis in utero is intrauterine growth restriction (IUGR). Few studies showed reduced weight of the fetal kidney in IUGR fetuses as compared to normally grown fetuses. Reduced blood flow to the kidneys due to fetal hypoxemia in IUGR foetus leads to increased pulsatility index which is likely to be responsible for impaired nephrogenesis and decreased kidney volume. AIMS AND OBJECTIVE: To estimate if fetal renal artery Doppler could affect fetal renal volume in healthy and growth restricted fetuses after 26 weeks of gestation. STUDY DESIGN AND SETTING: Cross sectional study carried out in the Department radio diagnosis, Lata Mangeshkar hospital, Nagpur, Maharashtra, India. MATERIAL AND METHODS: Total 336 patients, which consisted of 309 normally grown fetuses and 27 intrauterine growth restricted fetuses were included in the study. Fetal renal volume of individual kidney, combined renal volume and relative renal volumes were calculated using 2 dimensional ultrasound for normal and IUGR fetuses. Fetal renal artery parameters particularly renal arterial pulsatility index were calculated for both the groups. Correlation of fetal renal Doppler parameters with renal volume was estimated for respective groups. RESULTS: Combined kidney volume was significantly reduced in growth restricted fetuses than normal fetuses i.e. mean combined kidney volume for growth restricted fetuses was 12.6cc and for normal fetuses was 19.29cc. Most of the fetal biometric indices were positively correlated with the combined kidney volume. Increased pulsatility index was seen in growth restricted fetuses i.e. on right side 1.37+/-0.35 and on left 1.40+/-0.35 i.e. >1 while for normal fetuses was 0.88 +/-0.08 on either side i.e. <1. Considerable negative correlation was found between fetal renal artery pulsatility index and renal volume. CONCLUSION: Increased fetal renal artery pulsatility index in intrauterine growth restricted fetuses is negatively correlated with renal volume resulting in reduced renal perfusion and impaired nephrogenesis.