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Plasma 17-hydroxyprogesterone in newborn infants with congenital adrenal hyperplasia and in infants with normal adrenal function

机译:先天性肾上腺皮质增生的新生儿和肾上腺功能正常的婴儿的血浆17-羟孕酮

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摘要

Plasma 17-hydroxyprogesterone (17-OHP) was estimated in 9 infants aged 6 to 12 days with congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. Raised plasma 17-OHP values, ranging from 3·4 to 25·0 μg/100 ml were found. 50 infants aged 10 hours to 15 days with normal adrenal function were also studied. One infant with galactosaemia had 17-OHP levels of 1·8 and 2·4 μg/100 ml, and a further 3 infants aged 15 hours to 3 days had 17-OHP levels between 1·1 and 2·1 μg/100 ml. In the remaining infants, plasma 17-OHP was less than 1·0 μg/100 ml. It therefore appears that estimation of plasma 17-OHP provides a useful method for confirming the diagnosis of CAH during the newborn period.
机译:估计9名6至12天的婴儿因21-羟化酶缺乏而患有血浆17-羟孕酮(17-OHP)。发现升高的血浆17-OHP值范围为3·4至25·0μg/ 100 ml。还研究了50名年龄在10小时至15天的肾上腺功能正常的婴儿。 1名半乳糖血症婴儿的17-OHP水平为1·8和2·4μg/ 100 ml,另外3名15小时至3天的婴儿的17-OHP水平在1·1至2·1μg/ 100 ml之间。在其余婴儿中,血浆17-OHP小于1·0μg/ 100 ml。因此,血浆17-OHP的估算似乎为确认新生儿期CAH的诊断提供了一种有用的方法。

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