Clinicopathological and genetic features of Zinner’s syndrome: two case reports and review of the literature

Ruijie Dai; Fan Jiang; Junjie Fan; Dalin He; Lei Li; Kaijie Wu

doi:10.3389/fruro.2023.1257368

Clinicopathological and genetic features of Zinner’s syndrome: two case reports and review of the literature

Ruijie Dai
, Fan Jiang
, Junjie Fan
, Dalin He
, Lei Li
, Kaijie Wu

The First Affiliated Hospital of Xi’an Jiaotong University
Baoji Central Hospital

科研成果: 期刊稿件 › 文章 › 同行评审

6 引用（Scopus）

摘要

Zinner’s syndrome (ZS) is a rare congenital malformation due to abnormal development of the urogenital tract. It is characterized by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. Cases are rarely reported in China since the incidence of the disease is low. Symptoms also vary widely among patients and its etiology is unclear. In this article, we described two patients with totally different cinicopathological and genetic features based on exon sequencing.

源语言	英语
期刊论文编号	1257368
期刊	Frontiers in Urology
卷	3
DOI	https://doi.org/10.3389/fruro.2023.1257368
出版状态	已出版 - 2023
已对外发布	是

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abstract = "Zinner{\textquoteright}s syndrome (ZS) is a rare congenital malformation due to abnormal development of the urogenital tract. It is characterized by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. Cases are rarely reported in China since the incidence of the disease is low. Symptoms also vary widely among patients and its etiology is unclear. In this article, we described two patients with totally different cinicopathological and genetic features based on exon sequencing.",

keywords = "Zinner{\textquoteright}s syndrome, exon sequencing, genetic mutation, seminal vesicle cyst, unilateral renal dysplasia",

author = "Ruijie Dai and Fan Jiang and Junjie Fan and Dalin He and Lei Li and Kaijie Wu",

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year = "2023",

doi = "10.3389/fruro.2023.1257368",

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T1 - Clinicopathological and genetic features of Zinner’s syndrome

T2 - two case reports and review of the literature

AU - Dai, Ruijie

AU - Jiang, Fan

AU - Fan, Junjie

AU - He, Dalin

AU - Li, Lei

AU - Wu, Kaijie

PY - 2023

Y1 - 2023

N2 - Zinner’s syndrome (ZS) is a rare congenital malformation due to abnormal development of the urogenital tract. It is characterized by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. Cases are rarely reported in China since the incidence of the disease is low. Symptoms also vary widely among patients and its etiology is unclear. In this article, we described two patients with totally different cinicopathological and genetic features based on exon sequencing.

AB - Zinner’s syndrome (ZS) is a rare congenital malformation due to abnormal development of the urogenital tract. It is characterized by the triad of unilateral renal agenesis, ipsilateral seminal vesicle cyst and ipsilateral ejaculatory duct obstruction. Cases are rarely reported in China since the incidence of the disease is low. Symptoms also vary widely among patients and its etiology is unclear. In this article, we described two patients with totally different cinicopathological and genetic features based on exon sequencing.

KW - Zinner’s syndrome

KW - exon sequencing

KW - genetic mutation

KW - seminal vesicle cyst

KW - unilateral renal dysplasia

UR - https://www.scopus.com/pages/publications/85183177801

U2 - 10.3389/fruro.2023.1257368

DO - 10.3389/fruro.2023.1257368

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AN - SCOPUS:85183177801

SN - 2673-9828

VL - 3

JO - Frontiers in Urology

JF - Frontiers in Urology

M1 - 1257368

ER -

Clinicopathological and genetic features of Zinner’s syndrome: two case reports and review of the literature

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