Huot C, Gauthier M, Lebel M, Larbrisseau A
Department of Pediatrics, Hôpital Sainte-Justine, University of Montréal, Québec, Canada.
Can J Neurol Sci. 1987 Aug;14(3):290-3. doi: 10.1017/s0317167100026639.
Two children born with birth defects after intrauterine exposure to valproic acid are reported. The mothers took the drug throughout pregnancy as sole treatment for primary generalized epilepsy. The first baby showed facial dysmorphism, arachnodactyly and triphalangeal thumbs. The second had facial dysmorphism, severe laryngeal hypoplasia, tracheomalacia and an aberrant innominate artery that caused tracheal compression. A left superior vena cava, abnormal pulmonary lobulation, and unilateral hydronephrosis were also found at autopsy. Valproic acid has probable teratogenic potential in humans but the number of reported cases is few and the spectrum of anomalies is broad so it is not possible to delineate a definite fetal valproate syndrome.
据报道,有两名儿童在子宫内接触丙戊酸后出生时患有出生缺陷。母亲在整个孕期都服用该药物,作为原发性全身性癫痫的唯一治疗方法。第一个婴儿表现出面部畸形、蜘蛛指和拇指三节指骨。第二个婴儿有面部畸形、严重的喉发育不全、气管软化以及一条异常的无名动脉导致气管受压。尸检还发现有左上腔静脉、异常肺小叶形成和单侧肾积水。丙戊酸在人类中可能有致畸潜力,但报告的病例数量很少,且异常情况的范围很广,因此无法明确界定一种特定的胎儿丙戊酸盐综合征。