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Features include: Omphalocele.
No clinical trials have been registered for omphalocele, X-linked.
5 publications have been identified in PubMed for omphalocele, X-linked. Research spans Case Report / Case Series (100%).
Wagner SA (2026). [PMID: 41748205](https://pubmed.ncbi.nlm.nih.gov/41748205/). *Neonatal Netw*. [Case Report / Case Series]
Schwarz M (2026). [PMID: 40884164](https://pubmed.ncbi.nlm.nih.gov/40884164/). *Clin Genet*. [Case Report / Case Series]
Wu YJ (2025). [PMID: 40678017](https://pubmed.ncbi.nlm.nih.gov/40678017/). *Surg Case Rep*. [Case Report / Case Series]
Fabijan A (2024). [PMID: 38786301](https://pubmed.ncbi.nlm.nih.gov/38786301/). *Diagnostics (Basel)*. [Case Report / Case Series]
Zhang W (2024). [PMID: 39091686](https://pubmed.ncbi.nlm.nih.gov/39091686/). *Front Nutr*. [Case Report / Case Series]
Data assembled from 4 of 12 sources · Last updated Sep 18, 2026, 5:26 PM UTC
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
AI-curated news mentioning omphalocele, X-linked
Updated Jun 4, 2026
A case report highlights an unusual omphalocele associated with Cantrell syndrome, contributing to the understanding of this rare condition. This report may provide insights for clinicians dealing with similar cases.