TY - CHAP M1 - Book, Section TI - King-Denborough Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164075320 ER -