RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164075320 T1 King-Denborough 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=1164075320 RD 2024/03/28 AB It is a rare medical condition characterized by the presence of a triad of dysmorphic craniofacial and skeletal abnormalities, malignant hyperthermia susceptibility (MHS), and myopathy. The myopathy is associated with Noonan-like features. However, in contrast to Noonan Syndrome, there is no congenital heart disease, mental retardation, or webbed neck (pterygium colli). Serum creatinine kinase (CK) might be elevated. Males are affected five times more often than females.