A novel DCC truncating mutation leads to rare congenital mirror movements and corpus callosum agenesis: A case report
These findings expand the spectrum of DCC mutations associated with MRMV1 and ACC, contributing to genetic counseling and prenatal diagnosis for MRMV patients, and shedding light on the role of DCC in neurodevelopment.
Authors
- Aiqian Zhang (ORCID: https://orcid.org/0000-0001-5680-2529)
- Lulu Tang (ORCID: https://orcid.org/0000-0002-4941-842X)
- Jianyin Yin (ORCID: https://orcid.org/0009-0004-1086-0757)
- Yi Dong (ORCID: https://orcid.org/0000-0002-3709-6566)
- Liang‐Liang Fan (ORCID: https://orcid.org/0000-0001-7431-1838)
- Yali Li (ORCID: https://orcid.org/0000-0002-9494-8462)
- Gaohui Cao
Institutions
- Central South University (CN)
- London Rebuilding Society (GB)
- Hebei General Hospital (CN)
- Third Xiangya Hospital (CN)
- Hunan Provincial Maternal and Child Health Hospital (CN)
- S.P.E.C.I.E.S. (US)
Publication Details
- Journal
- Medicine
- Published
- 2025-11-14
- DOI
- https://doi.org/10.1097/md.0000000000045836
- Primary Topic
- Fetal and Pediatric Neurological Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00