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2
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本文引用的文献

1
Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia.先天性肾上腺皮质增生症 21 羟化酶缺乏症。
Pediatr Clin North Am. 2011 Oct;58(5):1281-300, xii. doi: 10.1016/j.pcl.2011.07.012.
2
Congenital adrenal hyperplasia.先天性肾上腺增生症
J Pediatr Adolesc Gynecol. 2011 Jun;24(3):116-26. doi: 10.1016/j.jpag.2010.10.001.
3
Gender role behaviour in prenatally dexamethasone-treated children at risk for congenital adrenal hyperplasia--a pilot study.先天性肾上腺皮质增生症高危儿产前地塞米松治疗后的性别角色行为——一项初步研究。
Acta Paediatr. 2011 Sep;100(9):e112-9. doi: 10.1111/j.1651-2227.2011.02260.x. Epub 2011 Apr 8.
4
Non-invasive prenatal diagnosis.
Methods Mol Biol. 2011;688:155-72. doi: 10.1007/978-1-60761-947-5_11.
5
Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline.先天性肾上腺皮质增生症由类固醇 21-羟化酶缺乏引起:内分泌学会临床实践指南。
J Clin Endocrinol Metab. 2010 Sep;95(9):4133-60. doi: 10.1210/jc.2009-2631.
6
Prenatal dexamethasone use for the prevention of virilization in pregnancies at risk for classical congenital adrenal hyperplasia because of 21-hydroxylase (CYP21A2) deficiency: a systematic review and meta-analyses.产前使用地塞米松预防因 21-羟化酶(CYP21A2)缺陷而导致经典先天性肾上腺皮质增生症风险的妊娠女性出现男性化:系统评价和荟萃分析。
Clin Endocrinol (Oxf). 2010 Oct;73(4):436-44. doi: 10.1111/j.1365-2265.2010.03826.x.
7
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A paradigm for prenatal diagnosis and treatment.先天性肾上腺皮质增生症 21-羟化酶缺乏症:产前诊断和治疗的范例。
Ann N Y Acad Sci. 2010 Mar;1192:5-11. doi: 10.1111/j.1749-6632.2009.05225.x.
8
Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.21-羟化酶缺陷所致非经典型先天性肾上腺皮质增生症妇女的生育能力。
J Clin Endocrinol Metab. 2010 Mar;95(3):1182-90. doi: 10.1210/jc.2009-1383. Epub 2010 Jan 15.
9
Reassessing fecundity in women with classical congenital adrenal hyperplasia (CAH): normal pregnancy rate but reduced fertility rate.重新评估经典型先天性肾上腺皮质增生症(CAH)女性的生育力:妊娠率正常但生育率降低。
Clin Endocrinol (Oxf). 2009 Jun;70(6):833-7. doi: 10.1111/j.1365-2265.2009.03563.x. Epub 2009 Feb 25.
10
Prenatal diagnosis and treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.21-羟化酶缺乏所致先天性肾上腺皮质增生症的产前诊断与治疗
Mol Cell Endocrinol. 2009 Mar 5;300(1-2):192-6. doi: 10.1016/j.mce.2008.11.027. Epub 2008 Dec 3.

孕期先天性肾上腺皮质增生症:处理方法取决于“患者”是谁。

Congenital adrenal hyperplasia in pregnancy: approach depends on who is the 'patient'.

作者信息

Keely Erin, Malcolm Janine

机构信息

Departments of Medicine and Obstetrics/Gynecology, University of Ottawa, Ottawa ON, Canada.

出版信息

Obstet Med. 2012 Dec;5(4):154-160. doi: 10.1258/om.2012.120015. Epub 2012 Sep 24.

DOI:10.1258/om.2012.120015
PMID:30705696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6341502/
Abstract

Congenital adrenal hyperplasia (CAH) is a group of autosomal-recessive disorders caused by a reduced or absent enzymatic activity at one of the stages of adrenal steroid biosynthesis. Prenatal exposure to androgens leads to external genital masculinization of the affected female child. In pregnancy, the provider may be optimizing care for the woman with CAH or targeting treatment to reduce virilization in the affected unborn child. For the affected adult woman the goals of therapy in pregnancy are to prevent adrenal insufficiency, reduce fetal exposure to androgens and glucocorticoids and to avoid damage to reconstructed genitalia. For prenatal therapy for prevention of virilization of possibly affected female children, dexamethasone is used. However, questions remain about the efficacy and safety of exposing 7/8 unaffected children in the first trimester. Prenatal treatment should only be undertaken after careful discussion with the parents of the risks and benefits in an experienced centre or as part of a research protocol.

摘要

先天性肾上腺皮质增生症(CAH)是一组常染色体隐性疾病,由肾上腺类固醇生物合成某一阶段酶活性降低或缺乏所致。产前暴露于雄激素会导致患病女童外生殖器男性化。在孕期,医疗服务提供者可能会优化对患有CAH的女性的护理,或采取针对性治疗以减少患病胎儿的男性化。对于成年患病女性,孕期治疗的目标是预防肾上腺功能不全,减少胎儿暴露于雄激素和糖皮质激素,并避免对重建的生殖器造成损伤。为预防可能患病的女童男性化而进行产前治疗时,使用地塞米松。然而,关于在孕早期让7/8未患病胎儿暴露于此治疗的有效性和安全性仍存在疑问。产前治疗应仅在经验丰富的中心与父母仔细讨论风险和益处后进行,或作为研究方案的一部分开展。