RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164074849 T1 Katz Syndrome T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accessanesthesiology.mhmedical.com/content.aspx?aid=1164074849 RD 2024/03/29 AB It is an inherited polymalformative syndrome characterized by typical facial features, enlarged viscera, and skeletal anomalies. Other features include short stature, cranial hyperostosis, hepatomegaly, and diabetes mellitus. It is probably a variant of autosomal recessive type of craniometaphyseal dysplasia.