ArticleUrology case reports2021
Zinner's syndrome: Case report of a rare maldevelopment in the male genitourinary tract.
Article in Urology case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Zinner syndrome incidentally diagnosed in a man with ureteropelvic junction stone and hydronephrosis: A case report.Urology case reports · 2025Article
- Zinner syndrome with contralateral hydronephrosis: A rare congenital condition.Urology case reports · 2024Article
- Case Report: Incidental finding of Zinner syndrome in an asymptomatic 53-year-old Palestinian male.Frontiers in urology · 2023Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Zinner syndrome is a rare congenital malformation of the urogenital tract. It is due anomaly in the developmental of Wolffian duct. Zinner syndrome comprises triad of seminal vesicle cyst, unilateral renal agenesis and ipsilateral ejaculatory duct obstruction. It is frequently associated with infertility. Herein we are highlighting a case of a 35 years-old male, a father of 4 biological children who presented to our clinic due to right hemiscrotal pain, associated with post ejaculation pain.
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