Zinner Syndrome Cn305467
A rare congenital condition in males where one kidney and nearby reproductive structures fail to develop. It may cause urinary symptoms and requires monitoring.
Key facts at a glance
- ICD-10
- N39.0
- ICD-11
- GA00.0
- Body system
- genitourinary
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(genitourinary)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Hematospermia
(genitourinary)Perineal pain
(genitourinary)Dysuria
(genitourinary)Infertility
(genitourinary)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Conservative observation for asymptomatic cases
Asymptomatic patients with incidentally discovered Zinner syndrome typically require only periodic imaging surveillance to monitor for developing complications.
Antibiotic therapy for infectious complications
Prolonged antibiotic courses for recurrent seminal vesicle or prostatic infections common in Zinner syndrome due to obstructed drainage.
Additional treatment options
Laparoscopic seminal vesicle excision
Minimally invasive surgical removal of symptomatic cystic seminal vesicles causing pain, infection, or urinary symptoms refractory to conservative management.
surgicalTransrectal ultrasound-guided drainage
Image-guided percutaneous drainage of infected seminal vesicle cysts, providing both therapeutic benefit and diagnostic specimens for culture.
procedureFertility counseling and assisted reproduction consultation
Specialized reproductive urology consultation for males with obstructive azoospermia, exploring sperm retrieval and assisted reproductive techniques.
complementaryWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Zinner Syndrome Cn305467?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Pallwein L, Krestan C, Ponholzer A, et al. Zinner Syndrome: A Rare Developmental Anomaly of the Mesonephric Duct. Urologia Internationalis. 2018.
European Association of Urology. Urogenital Anatomy Abnormalities: Clinical Management Guidelines. Eur Urol Suppl. 2020.
Denison FJ, Omerbasir M, Patel RV. Clinical Presentation and Management of Zinner Syndrome: A Case Series and Literature Review. Journal of Clinical Urology. 2019.
Kumar S, Ammar H, Fujiwara M. Imaging Features of Zinner Syndrome and Associated Complications on Multiplanar Imaging. Abdominal Radiology. 2022.
Medication Comparisons
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View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy