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Updated: Sep 27, 2025

Laparoscopic Oocyte Retrieval and Cryopreservation during Vaginoplasty for Treatment of Mayer-Rokitansky-Kuster-Hauser Syndrome
Published on: May 10, 2022
[And there was Zinner's syndrome-a rare differential diagnosis]
Christina Grund1, Victoria Margaux Krieg2, Joachim Leißner2
1Urologgia, Urologie im Helios Haus, Venloer Str. 389, 50825, Köln, Deutschland. post@urologgia.de.
Abstract:
Zinner's syndrome is a rare congenital abnormality of the Wolffian ducts in male patients. It consists of the triad of renal agenesis, ipsilateral seminal vesicle dilatation, and obstruction of the ejaculatory duct. Symptoms often occur after puberty and can include hematospermia, painful ejaculation, dysuria, and local discomfort. We present the case of a 15-year-old patient with this rare condition who was treated surgically after the diagnosis was confirmed.
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