26 June 2022
: Case report
Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation
Challenging differential diagnosis, Rare disease, Congenital defects / diseases
Pongsakorn Choochuen1ABCDEF, Wison Laochareonsuk12CD, Pattama Tanaanantarak3CD, Kanet Kanjanapradit4B, Surasak Sangkhathat25ADEG*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.