TY - CHAP M1 - Book, Section TI - Acrocephalosyndactyly Syndromes A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A group of diseases characterized by craniofacial anomalies with dysmorphic facial features mainly resulting from premature craniosynostosis and by hand and foot anomalies most often consisting of brachy-, syn-, and polysyndactyly. A number of subtypes exist, but considerable phenotypic overlap occurs with experts now considering many of these syndromes to represent variants of the same disease. The classification into subtypes in the literature is conflicting. Furthermore, the Acrocephalosyndactyly and Acrocephalopolysyndactyly Syndromes have overlapping features and the classification, by many considered a pseudo-distinction, has been changed a few times since the first description. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164060288 ER -