Prenatal diagnosis, ultrasound findings and pregnancy outcome of 7q11.23 deletion and duplication syndromes: what are the fetal features?
Our study broadened the clinical phenotype spectrum of fetuses with 7q11.23 deletions and duplications. Additionally, it conducted a preliminary evaluation of prenatal ultrasound findings and postnatal clinical phenotypes in follow-up cases. The clinical phenotype of fetuses with 7q11.23 deletion and duplication syndromes involves multiple systems and is relatively complex. Cardiovascular abnormalities and intrauterine growth restriction are the most common clinical manifestations observed in prenatal 7q11.23 deletion syndrome. Fetuses with 7q11.23 duplications exhibit a wide range of clinical phenotypes that lack specificity.
Authors
- Yuanyuan Pei (ORCID: https://orcid.org/0000-0002-9283-5958)
- Weiqiang Liu (ORCID: https://orcid.org/0000-0001-8398-8648)
- Xiaojin Luo (ORCID: https://orcid.org/0000-0001-6882-4194)
- Fei Zhou (ORCID: https://orcid.org/0000-0003-1216-2181)
- Hongyan Niu (ORCID: https://orcid.org/0009-0005-0860-3687)
- Fengxiang Wei (ORCID: https://orcid.org/0009-0006-6324-8400)
- Xiaohang Chen
Institutions
- Shantou University (CN)
- Shenzhen Maternity and Child Healthcare Hospital (CN)
Publication Details
- Journal
- BMC Pregnancy and Childbirth
- Published
- 2024-11-06
- DOI
- https://doi.org/10.1186/s12884-024-06920-2
- Citations
- 1
- Primary Topic
- Congenital heart defects research
- Type
- article
- Field-Weighted Citation Impact
- 0.23