Pinto W, Gardner L I, Rosenbaum P
Am J Dis Child. 1977 Apr;131(4):452-5. doi: 10.1001/archpedi.1977.02120170078016.
Abnormal genitalia was a salient clinical finding in two unrelated male infants with the hydantoin embryopathy syndrome. Both infants also exhibited hypoplastic nails of fingers and toes, hypertelorism, and a flat nasal bridge, and one had severe developmental retardation. We review previously reported cases of the hydantoin embrypathy syndrome and discuss factors possibly affecting the teratogenicity of phenytoin. Male infants with findings such as the patients of this report need to be differentiated from patients with Noonan syndrome and Aarskog syndrome. We suggest that mothers receiving phenytoin who have given birth to one affected infant should be given a different anticonvulsant for future pregnancies.
生殖器异常是两名患有苯妥英胚胎病综合征的无血缘关系男婴的显著临床特征。两名婴儿还均表现出手指和脚趾指甲发育不全、眼距增宽以及鼻梁扁平,其中一名有严重发育迟缓。我们回顾了先前报道的苯妥英胚胎病综合征病例,并讨论了可能影响苯妥英致畸性的因素。有本报告中患者这类表现的男婴需要与努南综合征和阿斯克格综合征患者相鉴别。我们建议,生育过一名患病婴儿的接受苯妥英治疗的母亲,未来怀孕时应换用其他抗惊厥药物。