Early genetic sequencing in neonates with hyperkalemia: a retrospective cross-sectional study
The genetic etiology of neonatal hyperkalemia is complex. When clinical manifestations involve risk factors, it is advisable to conduct hormone testing and provide symptomatic treatment. Early genetic testing can aid in the diagnosis of hyperkalemia and improve the treatment of neonates with atypical clinical manifestations.
Authors
- Yulan Lu (ORCID: https://orcid.org/0000-0003-4941-5736)
- Liyuan Hu (ORCID: https://orcid.org/0000-0003-2961-4025)
- Fanshu Xu
- Xiang Chen (ORCID: https://orcid.org/0000-0002-9800-6472)
- Hui Xiao (ORCID: https://orcid.org/0000-0002-9735-9081)
- Huiyao Chen (ORCID: https://orcid.org/0000-0003-4781-3941)
- Wenyi Liang (ORCID: https://orcid.org/0000-0003-2860-2911)
Institutions
- Children's Hospital of Fudan University (CN)
Publication Details
- Journal
- Translational Pediatrics
- Published
- 2025-02-01
- DOI
- https://doi.org/10.21037/tp-24-485
- Primary Topic
- Ion Transport and Channel Regulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00