女性21-羟化酶缺乏所致非经典型先天性肾上腺皮质增生症：诊断与治疗：2024年第11号 - Suppr

Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency in women: diagnosis and treatment: Number 11 - 2024.

作者信息

Nácul Andrea Prestes, Silva Ana Carolina Japur Sá Rosa E, Yela Daniela Angerame, de Medeiros Sebastião Freitas, Soares José Maria, Antoniassi Gabriela Pravatta Rezende, Damásio Lia Cruz da Costa, Maranhão Técia Maria de Oliveira, Maciel Gustavo Arantes Rosa, Benetti-Pinto Cristina Laguna

机构信息

Grupo Hospitalar Conceição Hospital Fêmina Porto AlegreRS Brazil Hospital Fêmina, Grupo Hospitalar Conceição, Porto Alegre, RS, Brazil.

Universidade de São Paulo Faculdade de Medicina de Ribeirão Preto Departamento de Ginecologia e Obstetrícia Ribeirão PretoSP Brazil Departamento de Ginecologia e Obstetrícia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brazil.

出版信息

Rev Bras Ginecol Obstet. 2024 Nov 25;46. doi: 10.61622/rbgo/2024FPS11. eCollection 2024.

DOI:10.61622/rbgo/2024FPS11

PMID:39678099

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11640052/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14b8/11640052/75b7f1c52996/1806-9339-rbgo-46-e-FPS11-gf01.jpg

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Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency in women: diagnosis and treatment: Number 11 - 2024.女性21-羟化酶缺乏所致非经典型先天性肾上腺皮质增生症：诊断与治疗：2024年第11号

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Secondary biosynthetic defects in women with late-onset congenital adrenal hyperplasia.迟发性先天性肾上腺增生症女性的继发性生物合成缺陷。

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WOMEN WITH NONCLASSIC CONGENITAL ADRENAL HYPERPLASIA HAVE GENDER, SEXUALITY, AND QUALITY-OF-LIFE FEATURES SIMILAR TO THOSE OF NONAFFECTED WOMEN.患有非经典先天性肾上腺增生症的女性在性别、性特征和生活质量方面与未受影响的女性相似。

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Steroid 21-hydroxylase deficiency (congenital adrenal hyperplasia).类固醇21-羟化酶缺乏症（先天性肾上腺皮质增生症）。

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Getting pregnant with congenital adrenal hyperplasia: Assisted reproduction and pregnancy complications. A systematic review and meta-analysis.患有先天性肾上腺皮质增生症的女性妊娠：辅助生殖与妊娠并发症。系统评价与荟萃分析。

Front Endocrinol (Lausanne). 2022 Aug 31;13:982953. doi: 10.3389/fendo.2022.982953. eCollection 2022.

Steroid Screening Tools Differentiating Nonclassical Congenital Adrenal Hyperplasia and Polycystic Ovary Syndrome.类固醇筛查工具区分非经典型先天性肾上腺皮质增生症和多囊卵巢综合征。

J Clin Endocrinol Metab. 2020 Aug 1;105(8). doi: 10.1210/clinem/dgaa369.

Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review.多囊卵巢综合征与非经典型先天性肾上腺皮质增生症：不同特征与共同发现。一项系统评价。

Front Endocrinol (Lausanne). 2019 Jun 19;10:388. doi: 10.3389/fendo.2019.00388. eCollection 2019.

Prenatal genetic testing and treatment for congenital adrenal hyperplasia.先天性肾上腺皮质增生症的产前遗传检测与治疗。

Fertil Steril. 2019 Jan;111(1):21-23. doi: 10.1016/j.fertnstert.2018.11.041.

Fertility in patients with nonclassical congenital adrenal hyperplasia.非经典型先天性肾上腺皮质增生症患者的生育能力。

Fertil Steril. 2019 Jan;111(1):13-20. doi: 10.1016/j.fertnstert.2018.11.023.

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-羟化酶缺陷引起：内分泌学会临床实践指南。

J Clin Endocrinol Metab. 2018 Nov 1;103(11):4043-4088. doi: 10.1210/jc.2018-01865.

Evaluation and Treatment of Hirsutism in Premenopausal Women: An Endocrine Society Clinical Practice Guideline.绝经前女性多毛症的评估和治疗：内分泌学会临床实践指南。

J Clin Endocrinol Metab. 2018 Apr 1;103(4):1233-1257. doi: 10.1210/jc.2018-00241.

17α-HYDROXYLASE DEFICIENCY IS AN UNDERDIAGNOSED DISEASE: HIGH FREQUENCY OF MISDIAGNOSES IN A LARGE COHORT OF BRAZILIAN PATIENTS.17α-羟化酶缺陷症是一种被漏诊的疾病：在巴西的一个大型患者队列中，误诊率很高。

Endocr Pract. 2018 Feb;24(2):170-178. doi: 10.4158/EP171987.OR. Epub 2017 Nov 16.

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Hum Reprod Update. 2017 Sep 1;23(5):580-599. doi: 10.1093/humupd/dmx014.

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Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency in women: diagnosis and treatment: Number 11 - 2024.

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