A 106 years have passed since Zinner's syndrome was first described and current
knowledge is still almost exclusively based on case reports. This article presents three …

The authors made an up‐to‐date review of the literature concerning the management of
Zinner's syndrome and evaluated a young patient with Zinner's syndrome who had …

Zinner's syndrome is a rare congenital malformation of the seminal vesicle and ipsilateral
upper urinary tract, due to developmental arrest in early embryogenesis of the Müllerian …

Introduction: Zinner syndrome is a rare developmental anomaly of the Wolffian
(mesonephric) duct which is characterized by a triad of obstruction of the ejaculatory duct …

We present the case of a 51-year-old male with Zinner syndrome, which is a rare disease,
resulting from an abnormal evolution of the mesonephric (Wolffian) duct. It consists in cystic …

Zinner syndrome (ZS) is a rare disorder that affects only men. It is characterized by a triad of
abnormalities, including unilateral renal agenesis, ipsilateral seminal vesicle cysts, and …

Background Zinner syndrome represents a rare congenital malformation of the urinary tract.
It comprises a constellation of Wolffian duct anomalies and is almost exclusively …

Introduction and objective: Zinner syndrome is a rare congenital abnormality of the
mesonephric duct (Wolffian) consisting of unilateral renal agenesis, seminal vesicle cyst and …

Zinner syndrome was first described in 1914 and represents the triad of unilateral renal
agenesis and ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction …

Zinner syndrome is a rare male genitourinary tract disorder associated with seminal vesicle
cysts and ipsilateral renal agenesis. Clinical presentation often involves symptoms of the …