Searchable abstracts of presentations at key conferences in endocrinology

ea0022oc6.3 | Bone | ECE2010

Six novel mutations in 25-hydroxyvitamin D3 1α hydroxylase gene in patients with pseudovitamin D deficiency rickets

Abeguile Genevieve , Coudray Nadia , Richard Nicolas , Linglart Agnes , Kottler Marie-Laure

Pseudovitamin D deficiency rickets also called vitamin D-deficiency rickets type 1 (VDDR 1) is an autosomal recessive disorder in which 25-hydroxyvitamin D3 1 alpha-hydroxylase gene (CYP27B1) is deficient. VDDR1 is characterized by hypocalcemia,hypophosphatemia elevated serum PTH levels and low or undetectable serum concentrations of 1,25(OH)2D.We screened for mutations CYP27B1 in ten individuals from seven unrelated families wit...