Low-Set Ears: A New Marker of Fetal Chromosomal Anomalies
Our study supports using LSE as a potential 2D-ultrasound marker for chromosomal anomaly detection. Studies with a larger sample size and in high-risk populations are warranted to prove its clinical utility before this marker can be included in prenatal screening protocols.
Authors
- A. Borrell (ORCID: https://orcid.org/0000-0002-4304-4797)
- Gloria Jalencas
- Cristina Lesmes-Heredia
- Joan Carles Ferreres (ORCID: https://orcid.org/0000-0001-7742-0239)
- Viviana P. Beltrán
- Josep Maria Manresa‐Domínguez (ORCID: https://orcid.org/0000-0001-8306-5798)
- Maria Iniguez‐Cruz
- Elisabet Baldrich-Martin
- Isabel Mazano
Institutions
- Ferrer Grupo (Spain) (ES)
- Departament de Salut (ES)
- Institut Universitari d'Investigació en Atenció Primària Jordi Gol (ES)
- Institute of Research and Innovation Parc Tauli (ES)
- Institut Català de la Salut (ES)
- Universitat de Barcelona (ES)
Publication Details
- Journal
- Fetal Diagnosis and Therapy
- Published
- 2025-11-11
- DOI
- https://doi.org/10.1159/000548946
- Primary Topic
- Prenatal Screening and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 0.00