TY - CHAP M1 - Book, Section TI - Hypophosphatasia A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Hypophosphatasia (HPP) is a rare genetic disorder characterized by the abnormal development of bones (similar to vitamin D-resistant rickets) and teeth. Other features in this inherited inborn error of metabolism include failure to thrive, movement disorders, and low plasma levels of alkaline phosphatase. HPP is an extremely variable disorder. Six major clinical forms have been identified based primarily upon the age of onset of symptoms and diagnosis. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164073495 ER -