EPHB4 Mutation Suppresses PROX1 Expression and Disrupts Lymphatic Development in Neonatal Hydrops.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 35178555.
- Also identified by DOI 10.1542/peds.2021-053294.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
This case report highlights the importance of screening for mutations in EPHB4 and other genes that regulate lymphatic development in infants with the nonimmune hydrops fetalis.
Medical subject headings
- Homeodomain Proteins
- Hydrops Fetalis
- Receptor, EphB4
- Tumor Suppressor Proteins