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An instance of ossifying fibroma (disease) that is caused by an inherited modification of the individual's genome.
Features include: Tooth malposition, Multiple impacted teeth, and Cementoma.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for familial ossifying fibroma.
5 publications have been identified in PubMed for familial ossifying fibroma. Research spans Review / Meta-Analysis (40%), Case Report / Case Series (40%), and Basic Science / Preclinical (20%).
Wang Y (2026). [PMID: 41633608](https://pubmed.ncbi.nlm.nih.gov/41633608/). *Beijing Da Xue Xue Bao Yi Xue Ban*. [Case Report / Case Series]
Serani F (2026). [PMID: 41533239](https://pubmed.ncbi.nlm.nih.gov/41533239/). *EJNMMI Res*. [Case Report / Case Series]
Walker K (2025). [PMID: 41010632](https://pubmed.ncbi.nlm.nih.gov/41010632/). *J Clin Med*. [Review / Meta-Analysis]
Qadir A (2025). [PMID: 41497294](https://pubmed.ncbi.nlm.nih.gov/41497294/). *Indian J Endocrinol Metab*. [Basic Science / Preclinical]
Anbiaee N (2025). [PMID: 40727153](https://pubmed.ncbi.nlm.nih.gov/40727153/). *Indian J Otolaryngol Head Neck Surg*. [Review / Meta-Analysis]
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 6:55 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center