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Urosepsis as the Index Presentation Unmasking Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome with Left Duplex Collecting System and Bilateral Obstructive Uropathy: A Case Report

2026-08-13

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<title>Abstract</title> <p>Background Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital disorder characterised by aplasia of Müllerian duct–derived structures, resulting in absence of the uterus and upper vagina in phenotypically normal 46,XX females. The Type II variant (MURCS association) is associated with renal tract anomalies in 20–30% of cases, including renal agenesis, ectopia, and dupli...

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Literature Corpus work: 77c6f9fc-e2b7-554e-a216-63f461df184a
DOI: 10.21203/rs.3.rs-10319102/v1

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Urosepsis as the Index Presentation Unmasking Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome with Left Duplex Collecting System and Bilateral Obstructive Uropathy: A Case ReportDOI 10.21203/rs.3.rs-10319102/v1Read

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