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法伯病的产前诊断。

Prenatal diagnosis of Farber's disease.

作者信息

Fensom A H, Benson P F, Neville B R, Moser H W, Moser A E, Dulaney J T

出版信息

Lancet. 1979 Nov 10;2(8150):990-2. doi: 10.1016/s0140-6736(79)92562-5.

Abstract

Two pregnancies at risk for Farber's disease were monitored with amiocentesis at 15 and 16 weeks' gestation. In the first pregnancy tested, cultured amniotic-cell ceramidase activity was 7.8% of the control mean and an affected fetus was predicted. The pregnancy was terminated at 22 weeks' gestation and the diagnosis was confirmed by the demonstration of considerably elevated renal and hepatic ceramide concentrations and severe reduction of ceramidase activity in fetal brain and cultured fibroblasts. In the second pregnancy tested, cultured amniotic-cell ceramidase activity was within the control range, and the prediction of an unaffected fetus was confirmed in the newborn.

摘要

对两例有患法伯病风险的妊娠,在妊娠15周和16周时进行了羊膜穿刺术监测。在首例接受检测的妊娠中,培养的羊膜细胞神经酰胺酶活性为对照均值的7.8%,预测胎儿患病。妊娠在22周时终止,通过证实胎儿肾脏和肝脏中神经酰胺浓度大幅升高以及胎儿脑和培养的成纤维细胞中神经酰胺酶活性严重降低,确诊了该病。在第二例接受检测的妊娠中,培养的羊膜细胞神经酰胺酶活性在对照范围内,新生儿证实为未受影响的胎儿。

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