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Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for Carey-Fineman-Ziter syndrome.
6 publications have been identified in PubMed for Carey-Fineman-Ziter syndrome. Research spans Basic Science / Preclinical (50%), Epidemiology / Natural History (33%), and Case Report / Case Series (17%).
Zhang Z (2026). [PMID: 40317819](https://pubmed.ncbi.nlm.nih.gov/40317819/). *Dev Dyn*. [Basic Science / Preclinical]
Rahman F (2025). [PMID: 39668186](https://pubmed.ncbi.nlm.nih.gov/39668186/). *Eur J Hum Genet*. [Case Report / Case Series]
Dhar S (2025). [PMID: 41321131](https://pubmed.ncbi.nlm.nih.gov/41321131/). *Biol Open*. [Basic Science / Preclinical]
Almpani K (2025). [PMID: 40611650](https://pubmed.ncbi.nlm.nih.gov/40611650/). *Cleft Palate Craniofac J*. [Epidemiology / Natural History]
Liberton DK (2024). [PMID: 38791829](https://pubmed.ncbi.nlm.nih.gov/38791829/). *Int J Environ Res Public Health*. [Epidemiology / Natural History]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:41 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Carey-Fineman-Ziter syndrome