hrp0082p3-d3-690 | Bone (2) | ESPE2014
Boros Emese
, Rothenbuhler Anya
, Haidar Hazar
, Prie Dominique
, Harvengt Pol
, Vija Lavinia
, Brailly-Tabard Sylvie
, Chanson Philippe
, Linglart Agnes
, Kamenicky Peter
Background: Hereditary hypophosphatemic rickets (HHR) is a rare genetic disease characterized by renal phosphate wasting, caused by elevated circulating FGF23. Despite the current available treatment complications include short stature, hyperparathyroidism, pseudofractures, bone pain, bone demineralization and osteoporosis, nephrocalcinosis and enthesopathies. Elevated circulating FGF23 was recently involved in glucose metabolism and cardiovascular function.<p class="abste...