A rare case of Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome with solitary ectopic pelvic kidney and uretropelvic junction (UPJ) obstruction-Reference-Cited by-同舟云学术

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A rare case of Mayer–Rokitansky–Kuster–Hauser (MRKH) syndrome with solitary ectopic pelvic kidney and uretropelvic junction (UPJ) obstruction

Published:2018-11 Issue: Volume:21 Page:113-115
ISSN:2214-4420
Container-title:Urology Case Reports
language:en
Short-container-title:Urology Case Reports

Author:

Bubishate Saleh,Saleh Iqbal,Hasan Rami M.^ORCID

Publisher

Elsevier BV

Subject

Urology

Reference4 articles.

1. The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina) – phenotypic manifestations and genetic approaches;Guerrier;J Negat Results Biomed,2006

2. Mayer–rokitansky–kuster–hauser type-B anomaly with MURCS association and gonadal dysgenesis;Dasgupta;J Obstet Gynaecol India,2012

3. Ureteral switch for bilateral ureteropelvic junction obstruction in a case of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome;Mubenga;Afr J Urol,2013

4. Management of an unusual case of atypical Mayer–Rokitansky–Kuster–Hauser syndrome, with unilateral gonadal agenesis, solitary ectopic pelvic kidney, and pelviureteric junction obstruction;Kumar;International Urogynecology Journal,2006

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. Mayer-Rokitansky-Kuster-Hauser syndrome in a young female: diagnosis and treatment: a case report;Journal of the Pakistan Medical Association;2023-02-15

2. Aberrant DNA methylation in the PAX2 promoter is associated with Müllerian duct anomalies;Archives of Gynecology and Obstetrics;2020-04-18

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