Beckwith-Wiedemann综合征是比较罕见的染色体遗传疾病。国内虽有临床个案报道,但未曾有病理方面的描述。现将我院发现的2例报告如下: 2例死婴,系女性,第1胎。父母年龄均<30岁,非近亲婚配。家族中未见显性症状及体征。母孕期均有肝功能正常、血糖偏低(例1为73mg％;例2为69mg％)、血压升高、浮肿(+)的现象。婴儿 Beckwith-Wiedemann syndrome is a rare chromosomal genetic disease. Although there are clinical reports of domestic cases, but no pathological description. Now found in our hospital 2 cases are as follows: 2 dead baby, female, first child. Parents are <30 years old, non-relatives marriage. No dominant family symptoms and signs. Both pregnant women have normal liver function during pregnancy, low blood glucose (73mg% in case 1; 69mg% in case 2), elevated blood pressure and edema (+). baby