Mutations in FGF23. KL. and GALNT3 have been identified as the cause for the development of hyperphosphatemic familial tumoral calcinosis (HFTC). Patients with HFTC typically present in childhood or adolescence with periarticular soft tissue deposits that eventually progress to disrupt normal joint articulation. https://www.spidertattooz.com/WAC-4011-LED-Horizontal-Step-Light-Colorscaping/