TY - CHAP M1 - Book, Section TI - Weyers Syndrome II A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - This is a medical condition with an onset of symptoms at birth, affecting both sexes, and characterized by postaxial polydactyly of the hands and feet, hexadactyly and fusion of fifth and sixth metatarsals and metacarpals, as well as bony clefts of the mandibular symphysis. Other features include orodental anomalies, hypoplastic and dysplastic nails, short stature, micrognathia, small mouth, and hypoplasia of the larynx. Congenital heart defect may be present. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164088050 ER -