[Prenatal diagnosis and genetic analysis of two fetuses with Wolf-Hirschhorn syndrome].
The 4p deletion is probably the main cause for the WHS phenotype in both fetuses. WHS should be suspected when IUGR, renal anomalies, craniofacial and cardiovascular abnormalities are detected upon prenatal ultrasound screening.
Authors
- Mingxia Ma
- Jiang Tao Tang
- Suhuan Tang
- Weiguo Yin (ORCID: https://orcid.org/0000-0002-1318-9688)
- Xiaolei Xie (ORCID: https://orcid.org/0000-0001-5279-6045)
- Fuguang Li (ORCID: https://orcid.org/0000-0002-9057-0554)
- Weihe Tan
- Aijuan Wu
Institutions
- Xiyuan Hospital (CN)
- Guangzhou Medical University (CN)
Publication Details
- Journal
- PubMed
- Published
- 2024-10-10
- DOI
- https://doi.org/10.3760/cma.j.cn511374-20240306-00149
- Primary Topic
- Genomic variations and chromosomal abnormalities
- Type
- article