Genetic spectrum of unexplained neonatal seizures: a single-center study
Our findings demonstrate a high diagnostic yield of next-generation sequencing (NGS) in unexplained neonatal seizures and underscore its clinical utility in pinpointing treatable conditions and prognosticating severe disorders.
Authors
- Jinglin Xu (ORCID: https://orcid.org/0000-0002-6658-0058)
- Ruiquan Wang (ORCID: https://orcid.org/0000-0002-2365-5945)
- Tianfeng Chen (ORCID: https://orcid.org/0000-0001-6953-1342)
- Lin Wang (ORCID: https://orcid.org/0000-0001-5645-8991)
- Lianqiang Wu
- Yanling Zeng (ORCID: https://orcid.org/0000-0001-9485-2383)
- Ling Yu
- Hongyuan Yang
- Ying He
- Zhiyong Liu
- Cheng Cai
- Junzi Huang
Institutions
- Huaqiao University (CN)
- Quzhou City People's Hospital (CN)
- Wuhan College (CN)
- The 180th Hospital of PLA (CN)
- Shanghai Children's Hospital (CN)
Publication Details
- Journal
- Translational Pediatrics
- Published
- 2026-02-01
- DOI
- https://doi.org/10.21037/tp-2025-aw-750
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00