Van Maldergem syndrome-1 in a patient with central precocious puberty: A case report
This case highlights the hallmark clinical features of VMS-1, including neurodevelopmental impairment and craniofacial anomalies, while also expanding the known genetic spectrum of the disorder. These findings provide valuable insights into the diagnosis and management of this extremely rare genetic condition.
Authors
- Zubi Liu
- Yuxuan Dai
- Jiang Xiao-yun (ORCID: https://orcid.org/0000-0002-2071-6482)
- Yeping Wang (ORCID: https://orcid.org/0000-0002-8682-2456)
- Kaixuan Wang
- Lingjing Ying
- Bo Xu
Institutions
- Jingzhou Maternal and Child Health Hospital (CN)
- Dian Diagnostics (China) (CN)
- Jinhua Central Hospital (CN)
Publication Details
- Journal
- Medicine
- Published
- 2025-08-08
- DOI
- https://doi.org/10.1097/md.0000000000043550
- Primary Topic
- Sharing Economy and Platforms
- Type
- article
- Field-Weighted Citation Impact
- 0.00