TY - CHAP M1 - Book, Section TI - Miller Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a congenital disorder characterized by postaxial acrofacial dysostosis in association with severe postaxial limb deficiencies. The craniofacial malformations may include malar hypoplasia, micrognathia, cleft palate, small, protruding, “cup-shaped” ears, eye colobomas and ptosis, and ectropion. The limb abnormalities include incomplete hypoplasia, syndactyly, clinodactyly (eg, the fifth digits and, in some cases, the fourth and third digits), and hypoplasia of the ulna and occasionally the radius. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/11/09 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164078812 ER -