Hughes I A, Laurence K M
Lancet. 1979 Jul 7;2(8132):7-9. doi: 10.1016/s0140-6736(79)90174-0.
The concentration of 17-OH-progesterone (17-OHP) was measured retrospectively in a second-trimester amniotic-fluid sample obtained from a mother who had an infant with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. The concentration was more than three times the mean amniotic-fluid-17OHP concentration determined in pregnancies of comparable gestational age with normal outcome. In four further pregnancies tested, where the parents were heterozygous for CAH, amniotic-fluid concentrations of 17-OHP were normal. To date, three of the mothers have delivered normal infants. CAH can be detected in early pregnancy by specific radioimmunoassay techniques for steroid-hormone analysis in amniotic fluid. This antenatal test could be useful in those cases in which parents do not wish to risk having affected offspring.
对一名母亲孕中期羊水样本中的17-羟孕酮(17-OHP)浓度进行了回顾性测定,该母亲所生婴儿因21-羟化酶缺乏而患有先天性肾上腺皮质增生症(CAH)。该浓度超过了在具有正常结局的可比孕周妊娠中所测定的羊水17-OHP平均浓度的三倍。在另外四次检测的妊娠中,父母为CAH杂合子,羊水17-OHP浓度正常。迄今为止,其中三位母亲已分娩出正常婴儿。通过用于羊水类固醇激素分析的特定放射免疫测定技术,可以在妊娠早期检测出CAH。这种产前检测对于那些父母不希望有受影响后代风险的情况可能有用。