TY - CHAP M1 - Book, Section TI - Acrocephalosyndactyly Syndromes A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. Y1 - 2006 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - Group of diseases characterized by craniofacial anomalies resulting from premature sutural craniosynostosis and hand and foot anomalies consisting primarily of brachydactyly, syndactyly, and polysyndactyly. A number of different subtypes exist but considerable phenotypic overlap occurs, so investigators now consider many of these syndromes to represent variants of the same disease. The classification into subtypes in the literature is conflicting. Furthermore, the classification of acrocephalosyndactyly versus acrocephalopolysyndactyly is regarded by many as a pseudodistinction. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58061401 ER -