hrp0082p3-d1-660 | Bone | ESPE2014
Goksen Damla
, Ozen Samim
, Kitanaka Sachiko
, Isojima Tsuyoshi
, Cogulu Ozgur
, Darcan Sukran
Background: VDDR-II, is an autosomal recessive disorder characterized by the early onset of rickets with hypocalcemia, secondary hyperparathyroidism and hypophosphatemia and is caused by mutations in the vitamin D receptor (VDR) gene.Objective and hypotheses: 2 years old Turkish girl first offspring of consanguineous parents admitted to the hospital for the evaluation of total alopecia and bilaterally genu varum deformity. She was born with normal pilosi...