ArticleFrontiers in urology2023
Clinicopathological and genetic features of Zinner's syndrome: two case reports and review of the literature.
Article in Frontiers in urology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Zinner Syndrome: A Narrative Review of Imaging Findings with an Illustrative Case Report.Diagnostics (Basel, Switzerland) · 2026Review
- Zinner syndrome, a rare congenital urogenital tract malformation: the first reported case in Indonesia.Fukushima journal of medical science · 2025Article
- [Occlusive azoospermia in unilateral cystic alteration of the seminal vesicle and contralateral seminal vesicle agenesis-case report].Urologie (Heidelberg, Germany) · 2025Article
- Zinner syndrome: Clinical insights from Western Norway.Urologia · 2025Article
- Management Strategies for Seminal Vesicle Cysts in Zinner Syndrome: Insights From Two Cases.Cureus · 2025Article
- Zinner syndrome unveiled: Ectopic ureter and seminal vesicle cyst leading to urinary dysfunction: A case report.Radiology case reports · 2025Article
- A rare Zinner syndrome combined with testicular cancer: a case report.Frontiers in oncology · 2025Article
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Authors and funding
6 authors.
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Abstract
Zinner's syndrome (ZS) is a rare congenital malformation due to abnormal development of the urogenital tract. It is characterized by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. Cases are rarely reported in China since the incidence of the disease is low. Symptoms also vary widely among patients and its etiology is unclear. In this article, we described two patients with totally different cinicopathological and genetic features based on exon sequencing.
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