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Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for Greig cephalopolysyndactyly-contiguous gene syndrome.
2 publications have been identified in PubMed for Greig cephalopolysyndactyly-contiguous gene syndrome. Research spans Review / Meta-Analysis (50%) and Case Report / Case Series (50%).
Makay P (2025). [PMID: 39807610](https://pubmed.ncbi.nlm.nih.gov/39807610/). *Clinical dysmorphology*. [Case Report / Case Series]
Lazea C (2024). [PMID: 38791606](https://pubmed.ncbi.nlm.nih.gov/38791606/). *International journal of molecular sciences*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 9:43 PM UTC
European rare disease database
Common questions about Greig cephalopolysyndactyly-contiguous gene syndrome