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Voprosy praktičeskoj pediatrii, 2021
In this article, we report three cases of Zinner syndrome (renal agenesis or renal dysplasia, ipsilateral seminal vesicle cyst, and seminal duct obstruction) in children of different age and describe their diagnosis and treatment. All patients have undergone kidney and bladder ultrasonography, renal scintigraphy, and cystoscopy.
E.K. Ayryan +6 more
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In this article, we report three cases of Zinner syndrome (renal agenesis or renal dysplasia, ipsilateral seminal vesicle cyst, and seminal duct obstruction) in children of different age and describe their diagnosis and treatment. All patients have undergone kidney and bladder ultrasonography, renal scintigraphy, and cystoscopy.
E.K. Ayryan +6 more
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Zinner Syndrome with Ectopic Ureter Remnant
Current Medical Imaging Formerly Current Medical Imaging Reviews, 2022Introduction: Zinner syndrome is a rare congenital abnormality defined by a clinical triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction. Case Presentation: Most patients are asymptomatic, but if the cystic dilatation of the seminal vesicle becomes significant, it can result in urinary ...
Ara Ko +3 more
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Zinner Syndrome: A Radiological Case Report with Multimodal Imaging Insights
International Journal of Innovative Science and Research TechnologyBackground: Zinner Syndrome is a rare congenital condition of the male urogenital tract, defined by unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ejaculatory duct obstruction, resulting from mesonephric duct maldevelopment.
Vvt Sai Lekha +2 more
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Screening for Zinner Syndrome in Patients With a Congenitally Solitary Kidney: Lessons Learned
Journal of Urology, 2023Purpose: We determined if serial screening ultrasounds are beneficial in evaluating for the development of Zinner syndrome in males with a congenital solitary kidney.
E. Bearrick, D. Husmann
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Zinner syndrome: two cases and review of the literature
BMJ Case Reports, 2021Zinner syndrome (ZS) is a rare congenital malformation due to abnormal development of the urogenital tract. It is caused by a growth failure of the distal part of the Müllerian duct in early embryogenesis. It is characterised by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction.
Di Paola V. +3 more
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Ultrasonographic Appearance of Suspected Zinner Syndrome
Research PostersZinner syndrome (ZS) is a rare congenital condition characterized by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst, and ipsilateral ejaculatory duct obstruction.
W. Luo +4 more
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Zinner Syndrome: Modern Methods of Diagnosis and Treatment. Literature Review and Clinical Cases
Health of ManZinner syndrome (ZS) is a rare abnormality, described for the first time in 1914 by A. Zinner. The syndrome is caused by malformation of the ureteral bud at the early stages of embryogenesis, result in ipsilateral renal and the other structures anomalies
M. Sosnin +4 more
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[Robot-assisted vesiculectomy for Zinner syndrome].
UrologiiaThe association of congenital cysts of seminal vesicles with unilateral renal agenesis and obstruction of the vas deferens was first described by A.Zinner in 1914. Later, the combination of these anomalies was called Zinners syndrome.
Kamalov A.A. Kamalov +8 more
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Journal of Cancer Research and Therapeutics
Primary adenocarcinoma of the seminal vesicles is a rare tumor. Congenital seminal vesicle cysts are often associated with unilateral renal dysgenesis or agenesis (Zinner syndrome). Zinner syndrome is a rare congenital malformation represented by a group
Sheereen Fatima +2 more
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Primary adenocarcinoma of the seminal vesicles is a rare tumor. Congenital seminal vesicle cysts are often associated with unilateral renal dysgenesis or agenesis (Zinner syndrome). Zinner syndrome is a rare congenital malformation represented by a group
Sheereen Fatima +2 more
semanticscholar +1 more source
Zinner syndrome in a case of male infertility: a case report
International Surgery JournalZinner syndrome is a rare congenital malformation formed by the developmental anomaly of distal portion of the wolffian duct. It is an unusual cause of infertility and dysuria among young males.
R. M +3 more
semanticscholar +1 more source

