TY - CHAP M1 - Book, Section TI - Familial Osteodysplasia A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Inherited disorder believed to be an autosomal recessive trait. It is characterized by midface hypoplasia, malformation of the mandible, hypoplastic zygomatic bones, and abnormally pointed chin. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164069650 ER -