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    Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature

    Hyperphosphatemic familial tumoral calcinosis (HFTC), secondary to fibroblast growth factor 23 (FGF23) gene mutation, is a rare genetic disorder characterized by recurrent calcified masses. We describe young L...

    M. Chakhtoura, M.S. Ramnitz, N. Khoury, G. Nemer, N. Shabb… in Osteoporosis International (2018)