hrp0086p1-p125 | Bone & Mineral Metabolism P1 | ESPE2016
Acar Sezer
, Al-Rijjal Roua A.
, Demir Korcan
, Kattan Walaa E.
, Catli Gonul
, BinEssa Huda
, Abaci Ayhan
, Dundar Bumin
, Zou Minjing
, Kavukcu Salih
, Meyer Brian
, Bober Ece
, Shi Yufei
Background: There exists limited data regarding genetic etiology of hypophosphatemic rickets in Turkey.Objective and hypotheses: To investigate the type of genetic defect in 16 index children and their families (12 unrelated, 1 related).Method: Following clinical and laboratory assessment, PHEX analysis was made initially unless a mutation in another gene was suspected. If negative, FGF23, SLC34A3, SL...