A retrospective analysis of prenatal genetic results in fetal hydronephrosis
Hydronephrosis is associated with chromosomal abnormalities, and the rate of chromosomal abnormalities increases significantly as the degree of hydronephrosis increases. The combined use of CMA technology can detect abnormalities caused by chromosomal microdeletions and/or microduplications, which is of great value for clinical prenatal consultation.
Authors
- Xiayuan Xu
- Keqin Jin (ORCID: https://orcid.org/0000-0003-4309-4791)
- Min Hu (ORCID: https://orcid.org/0000-0002-6337-3969)
- Ping Zhang (ORCID: https://orcid.org/0000-0001-9163-6191)
- Yue Qian
- Jianfeng Luo (ORCID: https://orcid.org/0000-0002-9833-0416)
Institutions
- Jingzhou Maternal and Child Health Hospital (CN)
- Jinhua Academy of Agricultural Sciences (CN)
- Jinhua Central Hospital (CN)
Publication Details
- Journal
- PLoS ONE
- Published
- 2025-05-22
- DOI
- https://doi.org/10.1371/journal.pone.0324734
- Primary Topic
- Pediatric Urology and Nephrology Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Jinhua Science and Technology Bureau