Zinner's Syndrome: A Case Report with Typical Radiological Findings

Area of Science:

• Urology
• Embryology
• Genetics

Background:

• Zinner syndrome is a rare congenital anomaly of the male urogenital system.
• It arises from abnormal embryogenesis of the ureteric buds during fetal development.

Purpose of the Study:

• To describe the key features and embryological basis of Zinner syndrome.
• To highlight the typical clinical presentation and diagnostic considerations.

Main Methods:

• This is a descriptive summary based on existing literature.
• Review of case reports and embryological developmental pathways.

Main Results:

• Zinner syndrome is characterized by a triad of findings: unilateral renal agenesis, seminal vesicle cysts, and ipsilateral ejaculatory duct obstruction.
• The condition results from delayed development of the ureteric buds affecting nearby structures.

Conclusions:

• Zinner syndrome represents a rare but distinct urogenital malformation.
• Early recognition is crucial for appropriate management and understanding of its embryological origins.