A case report of an incidental finding of a 46,XX, SRY-negative male with masculine phenotype during standard fertility workup with review of the literature and proposed immediate and long-term management guidance-Reference-Cited by-同舟云学术

A case report of an incidental finding of a 46,XX, SRY-negative male with masculine phenotype during standard fertility workup with review of the literature and proposed immediate and long-term management guidance

Published:2013-04 Issue:5 Volume:99 Page:1273-1276
ISSN:0015-0282
Container-title:Fertility and Sterility
language:en
Short-container-title:Fertility and Sterility

Author:

Ryan Neil A.J.,Akbar Shahnaz

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology,Reproductive Medicine

Reference33 articles.

1. Chapelle A de la, Hortling H, Niemi M, Wennstrom J. XX sex chromosomes in a human male. First case. Acta Med Scand (Suppl) 1964;412:25–38.

2. Clinical, hormonal and cytogenic evaluation of 46 XX male and review of the literature;Ergun-Longmire;Pediatr Endocinol Metab,2005

3. Clinical, endocrinological and epigenetic features of the 46 XX male syndrome, compared with 47 XXY Klinefelter patients;Vorona;J Clin Endocrinol Metab,2007

4. Consensus statment on managment of intersex disorders;Hughes;J Pediatr Urol,2006

5. The etiology of male XX men;de la Chapelle;Hum Genet,1981

Cited by 7 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. A 46,XX karyotype in men with infertility: Two new cases and review of the literature;Journal of Human Reproductive Sciences;2022

2. A rare case of male sex reversal syndrome (46, XX) with negative SRY gene: a disorder of sexual differentiation (DSD);African Journal of Urology;2021-07-21

3. SRY-Positive 46-XX Testicular Disorder of Sex Development as a Rare Cause of Male Hypergonadotropic Hypogonadism: A Case Report;The Turkish Journal of Endocrinology and Metabolism;2021

4. 46,XX Testicular Disorder of Sex Development (DSD): A Case Report and Systematic Review;Medicina;2019-07-12

5. Expect the unexpected: screening for secondary findings in clinical genomics research;British Medical Bulletin;2017-04-07