Zinner syndrome: report of a case and whole exome sequencing
Zinner syndrome is a rare condition commonly diagnosed via various imaging modalities. Surgical resection remains the most effective treatment for symptomatic cases. Gene sequencing provides valuable insights into the genetic etiology of Zinner syndrome, enhancing our understanding and potentially guiding future diagnostic approaches.
Authors
- Yu Huang (ORCID: https://orcid.org/0000-0003-2730-5077)
- Chengcheng Wei (ORCID: https://orcid.org/0000-0002-6634-0572)
- Miao Wang (ORCID: https://orcid.org/0000-0002-0532-6312)
- Zhaohui Chen (ORCID: https://orcid.org/0000-0002-9472-2113)
- Feixiang Xu (ORCID: https://orcid.org/0000-0001-6722-228X)
- J. J. He (ORCID: https://orcid.org/0009-0009-4740-4532)
Institutions
- Union Hospital (HK)
- The Affiliated Yongchuan Hospital of Chongqing Medical University (CN)
- Huazhong University of Science and Technology (CN)
- Chongqing Medical University (CN)
Publication Details
- Journal
- Basic and Clinical Andrology
- Published
- 2025-03-11
- DOI
- https://doi.org/10.1186/s12610-025-00256-3
- Citations
- 4
- Primary Topic
- Urologic and reproductive health conditions
- Type
- article
- Field-Weighted Citation Impact
- 6.67