hrp0092p2-28 | Bone, Growth Plate and Mineral Metabolism | ESPE2019

Clinical Radiographic and Biochemical Findings of Three Patients with Hypophosphatasia Carrying the Same Mutation

Orbak Zerrin , Orbak Recep

Background: Hypophosphatasia (HP) is a rare inherited disorder characterized by defective bone and tooth mineralization and caused by deficiency in the tissue non-specific alkaline phosphatase gene (ALPL). The symptoms are remarkably variable in their clinical expression, and relate to numerous mutations in this gene.Aim: The purpose of this study was to document the clinical, biochemical and radiologic aspects of the th...