“…Histological studies had shown abundant shreds of evidence that the diseased placenta had considerably alteration in placental microstructures in which diseased placenta had increased syncytiotrophoblast apoptosis, fibrosis (Allaire et al, 2000 ; Roberts and Post, 2008 ; Scifres and Nelson, 2009 ; Güven et al, 2018 ), thicker trophoblast epithelium (Langheinrich et al, 2008 ), reduced elastin, and increased collagen (Macara et al, 1996 ; Wilhelm et al, 2002 ), suggesting that the mechanical properties of the placenta during disease could have been altered but no direct proof about the placenta mechanical properties was shown. Direct mechanical testing of normal and IUGR placenta was recently conducted and the mechanical properties of IUGR placenta were found to be stiffer than that of the normal placenta and the difference could be captured from constitutive models' parameters (Saw et al, 2018b ). However, the placenta stiffness difference was only significant at certain compression settings, suggesting that the use of non-invasive ultrasound elastography could be used in detecting disease placenta but the setting of placental elastography should be controlled wisely to enhance its' accuracy.…”