“…Although GMIVH is a rare event in the fetus, several investigators have detected GMIVH in utero using prenatal US and MRI [9,10,11,12,13,14,15,16,17,18,19,20,21,22]. In several cases, umbilical cord or placental abnormalities [14], maternal pancreatitis [17], maternal pre-eclampsia [11], maternal seizures [20], possible sex-linked disorders [18] and severe thrombocytopenia [18] have been implicated as the initiating factors in the pathogenesis of GMIVH, but in most cases no underlying disease was identified [23, 24]. In our case 1 of twins, only the one of the twins developed GMIVH, suggesting that systemic disorders such as maternal coagulopathies are not considered a significant factor, although fetal ‘focal’ coagulopathy could not be ruled out.…”