hrp0086p1-p125 | Bone & Mineral Metabolism P1 | ESPE2016

Spectrum of the Genetic Defects in Hypophosphatemic Rickets in A Group of Turkish Children

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...