TY - CHAP M1 - Book, Section TI - Lambert Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is a very rare inherited polymalformative syndrome characterized by the association between branchial arch dysplasia (malar hypoplasia, macrostomia, periauricular tags, meatal atresia, and clubfeet, inguinal hernia, and intrahepatic biliary atresia). Mental retardation is present. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/11/03 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164076224 ER -