hrp0082p2-d3-310 | Bone (2) | ESPE2014
Boros Emese
, Rothenbuhler Anya
, Heinrichs Claudine
, Brachet Cecile
, Esterle Laure
, Kamenicky Peter
, Harvengt Pol
, Brailly-Tabard Sylvie
, Haidar Hazar
, Gaucher Celine
, Silve Caroline
, Gossiome Charles
, Wicart Philippe
, Duplan Martin Biosse
, Courson Frederic
, Chaussain Catherine
, Linglart Agnes
Background: Hereditary Hypophosphatemic Rickets (HHR) is caused by persistently elevated FGF23 resulting in renal phosphate wasting and decreased 25 vitamin D hydroxylation. Treatment with vitamin D analogues (VDA) has been added to phosphate supplements in the late seventies.Objective and hypotheses: Our objective was to evaluate the outcomes of VDA and phosphate supplements in adult patients with HHR in comparison with patients who did not receive VDA ...