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26 June 2022: Articles

Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation

Challenging differential diagnosis, Rare disease, Congenital defects / diseases

Pongsakorn Choochuen A , Wison Laochareonsuk C , Pattama Tanaanantarak C , Kanet Kanjanapradit B , Surasak Sangkhathat A*

DOI: 10.12659/AJCR.935921

Am J Case Rep 2022; 23:e935921

Figure 1. Pedigree chart of the family. The affected patient is indicated by the arrow and filled square. The parents are consanguineous, as shown with a double horizontal line.

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923