Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and paratesticular leiomyomas: Case report and review of the literature-Reference-Cited by-同舟云学术

Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and paratesticular leiomyomas: Case report and review of the literature

Published:2013-02 Issue:1 Volume:9 Page:e31-e34
ISSN:1477-5131
Container-title:Journal of Pediatric Urology
language:en
Short-container-title:Journal of Pediatric Urology

Author:

Siminas S.,Kokai G.,Kenny S.E.

Publisher

Elsevier BV

Subject

Urology,Pediatrics, Perinatology, and Child Health

Reference19 articles.

1. Androgen resistance;Hughes;Best Pract Res Clin Endocrinol Metab,2006

2. Germ cell tumours in the intersex gonad: old paths, new directions, moving frontiers;Cools;Endocr Rev,2006

3. Testicular feminization syndrome and associated gonadal tumours in Denmark;Banksboll;Acta Obstetr et Gynecol Scandinav,1992

4. Genotype versus phenotype in families with androgen insensitivity syndrome;Boehmer;J Clin Endocrinol Metab,2001

5. Androgen receptor defects: syndromes of androgen insensitivity. Disorders of sex development: endocrine aspects;Bouvattier,2010

Cited by 11 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. Androgen Insensitivity Syndrome with Bilateral Gonadal Sertoli Cell Lesions, Sertoli–Leydig Cell Tumor, and Paratesticular Leiomyoma: A Case Report and First Systematic Literature Review;Journal of Clinical Medicine;2024-02-06

2. Risk of gonadal neoplasia in patients with disorders/differences of sex development;Cancer Epidemiology;2020-12

3. Features of the fetal gonad in androgen synthesis in the postpubertal testis are preserved in complete androgen insensitivity syndrome due to a novel genetic splice site donor variant in androgen receptor gene intron 1;The Journal of Steroid Biochemistry and Molecular Biology;2019-10

4. Case 29-2018: A 31-Year-Old Woman with Infertility;New England Journal of Medicine;2018-09-20

5. 46,XY disorder of sex development (DSD) due to 17β-hydroxysteroid dehydrogenase type 3 deficiency;The Journal of Steroid Biochemistry and Molecular Biology;2017-01