TY - CHAP M1 - Book, Section TI - Katz Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164074849 ER -