ERINATAL ARTERIAL ISCHEMIC stroke (PAS) is an important cause of cerebral palsy and other neurologic disabilities, including epilepsy and cognitive impairment. [1][2][3][4][5][6][7] Arterial ischemic stroke is diagnosed primarily in neonates born at term 8,9 and is responsible for 50% to 70% of congenital hemiplegic cerebral palsy in this population. 10,11 The cause of PAS is poorly understood. Investigators have reported a number of obstetric and neonatal complications in the setting of PAS, including birth asphyxia, preeclampsia, chorioamnionitis, cardiac anomalies, polycythemia, and systemic infection. 7,[12][13][14][15] Others have failed to find a significant difference in the frequency of perinatal complications between infants with PAS and controls. 1 6 Hematologic disorders, including factor V Leiden mutation and hyperhomocysteinemia, may also play a role in the pathogenesis of PAS. 14,[17][18][19] Previous studies of PAS are subject to a number of important limitations. Most describe only a small number of children 7,12,16,[20][21][22] or lack an adequate comparison group. 8,14,23 We found previously that preeclampsia and intrauterine growth restriction are independent risk factors for PAS. 15 However, our earlier