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Any acinar dysplasia in which the cause of the disease is a mutation in the FGF10 gene.
No clinical trials have been registered for acinar dysplasia caused by mutation in FGF10.
4 publications have been identified in PubMed for acinar dysplasia caused by mutation in FGF10. Research spans Basic Science / Preclinical (50%), Review / Meta-Analysis (25%), and Case Report / Case Series (25%).
Bzdęga K (2025). [PMID: 40145339](https://pubmed.ncbi.nlm.nih.gov/40145339/). *Am J Med Genet A*. [Basic Science / Preclinical]
Soreze YD (2025). [PMID: 41417852](https://pubmed.ncbi.nlm.nih.gov/41417852/). *PLoS One*. [Basic Science / Preclinical]
Szafranski P (2024). [PMID: 38044468](https://pubmed.ncbi.nlm.nih.gov/38044468/). *Pediatr Dev Pathol*. [Case Report / Case Series]
Tsujioka Y (2024). [PMID: 39012450](https://pubmed.ncbi.nlm.nih.gov/39012450/). *Jpn J Radiol*. [Review / Meta-Analysis]
Data assembled from 2 of 12 sources · Last updated Sep 18, 2026, 9:08 PM UTC
Common questions about acinar dysplasia caused by mutation in FGF10