RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164060288 T1 Acrocephalosyndactyly Syndromes T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164060288 RD 2024/03/29 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.