Journal Basic Info

  • Impact Factor: 1.995**
  • H-Index: 8
  • ISSN: 2474-1647
  • DOI: 10.25107/2474-1647
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Plastic Surgery
  •  Colon and Rectal Surgery
  •  Emergency Surgery
  •  Cardiovascular Surgery
  •  Endocrine Surgery
  •  Obstetrics Surgery
  •  Pediatric Surgery
  •  Gynecological Surgery


Citation: Clin Surg. 2021;6(1):3281.Case Report | Open Access

Zinner’s Syndrome: A Rare Case Series

Hiranya Deka, Rohit Kumar Singh and Appu Thomas*

Department of Urology, Amrita Institute of Medical Science, India

*Correspondance to: Appu Thomas 

 PDF  Full Text DOI: 10.25107/2474-1647.3281


Zinner’s syndrome is a very rare congenital condition characterized by seminal vesicle cyst, with upper tract anomaly-common being ipsilateral renal agenesis or renal dysplasia or ipsilateral congenital absence of vas deference is also present and obstruction of the ejaculatory duct. This condition would be a diagnostic challenge and its management at different age groups is also challenging as the indication for treatment will differ with age. Here we present a case series of two case of different age group with their different presentation and management strategies.


Cite the article

Deka H, Singh RK, Thomas A. Zinner’s Syndrome: A Rare Case Series. Clin Surg. 2021; 6: 3281.

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