The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene-Reference-Cited by-同舟云学术

The Presence of Clitoromegaly in the Nonclassical Form of 21-Hydroxylase Deficiency Could Be Partially Modulated by the CAG Polymorphic Tract of the Androgen Receptor Gene

Published:2016-02-05 Issue:2 Volume:11 Page:e0148548
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Moura-Massari Vivian Oliveira,Cunha Flávia Siqueira,Garcia Gomes Larissa,Bugano Diniz Gomes Diogo,Marcondes José Antônio Miguel,Madureira Guiomar,de Mendonca Berenice Bilharinho,Bachega Tânia A. Sartori Sanchez

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference59 articles.

1. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline;PW Speiser;J Clin Endocrinol Metab,2010

2. Congenital adrenal hyperplasia due to 21 hydroxylase deficiency: from birth to adulthood;PC White;Semin Reprod Med,2012

3. 21-Hydroxylase-deficient nonclassic adrenal hyperplasia is a progressive disorder: a multicenter study;C Moran;Am J Obstet Gynecol,2000

4. Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency;TA Bachega;J Clin Endocrinol Metab,1998

5. Comprehensive genetic analysis of 182 unrelated families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency;GP Finkielstain;J Clin Endocrinol Metab,2011

Cited by 10 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. The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant;Frontiers in Endocrinology;2023-02-14

2. Psychoendocrinology of congenital adrenal hyperplasia;Genetic Steroid Disorders;2023

3. Polymorphisms of androgens‐related genes and idiopathic male infertility in Turkish men;Andrologia;2021-10-10

4. The way toward adulthood for females with nonclassic congenital adrenal hyperplasia;Endocrine;2021-04-14

5. Challenges of CYP21A2 genotyping in children with 21-hydroxylase deficiency: determination of genotype–phenotype correlation using next generation sequencing in Southeastern Anatolia;Journal of Endocrinological Investigation;2021-03-06