Stangenberg M, Lingman G, Roberts G, Ozand P
Department of Obstetrics/Gynecology, King Faisal Hospital and Research Centre, Riyadh, Saudi Arabia.
Am J Med Genet. 1992 Sep 15;44(2):142-4. doi: 10.1002/ajmg.1320440205.
We report on fetal hydrops presenting at 18 weeks of gestation and diagnosed as beta-glucuronidase deficiency. The parents were first cousins and there were 2 previous similar fetal deaths. beta-Glucuronidase was absent in cultured fetal fibroblasts and lymphoblasts but was normal in the tested relatives. The activities of other lysosomal enzymes were normal.
我们报告了一例妊娠18周时出现胎儿水肿并被诊断为β-葡萄糖醛酸酶缺乏症的病例。父母为近亲结婚,此前有过2次类似的胎儿死亡。培养的胎儿成纤维细胞和淋巴细胞中缺乏β-葡萄糖醛酸酶,但检测的亲属中该酶正常。其他溶酶体酶的活性正常。