Primary amenorrhea in two sisters: description of a Mexican family with 17α hydroxylase-17 lyase deficiency caused by arginine

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Primary amenorrhea in two sisters: description of a Mexican family with 17α hydroxylase-17 lyase deficiency caused by arginine – stop mutation

Published:2012-02-06 Issue:9 Volume:28 Page:733-735
ISSN:0951-3590
Container-title:Gynecological Endocrinology
language:en
Short-container-title:Gynecological Endocrinology

Author:

Escamilla-Márquez Marco Antonio,Garduño-Garcia José de Jesús,Ordóñez-Sanchez Maria Luisa,Reza-Albarrán Alfredo,Tusie-Luna María Teresa,Gómez Pérez Francisco Javier,Aguilar-Salinas Carlos Alberto

Publisher

Informa UK Limited

Subject

Obstetrics and Gynecology,Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.tandfonline.com/doi/pdf/10.3109/09513590.2011.652718

Reference25 articles.

1. 17-hydroxylation deficiency in man.

2. The Role of Cytochrome b5 in the Biosynthesis of Androgens by Human P450c17

3. Steroid 17α-Hydroxylase Deficiency—Not Rare Everywhere

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Partial deficiency of 17α-hydroxylase: a rare cause of congenital adrenal hyperplasia;BMJ Case Reports;2019-12

2. Genetic defect of a combined 17 α-hydroxylase/17,20-lyase deficiency patient with adrenal crisis;Gynecological Endocrinology;2018-01-18

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