hrp0092p1-169 | Bone, Growth Plate and Mineral Metabolism (1) | ESPE2019
Paul Praveen George
, N.A Fouzia
, Korula Sophy
, Mathai Sarah
, George Biju
, Simon Anna
Introduction: Osteopetrosis (OP) is a rare genetic disorder that is characterized by abnormal osteoclast function resulting in dense bones and marrow failure. The only definitive cure for OP is stem cell transplantation (SCT). Hypercalcemia is a well described complication in children with OP undergoing SCT. This study describes the calcium profile and treatment modalities used to maintain normocalcemia in children with OP undergoing SCT.<p class="abstext"...