TY - CHAP M1 - Book, Section TI - Weaver 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 accelerated growth and osseous maturation, unusual craniofacial appearance, hoarse and low pitched cry, camptodactyly, and hypertonia. Most patients have muscle spasticity and exaggerated knee reflexes. There is an estimated risk in these children of less than or equal to 1.09% of rhabdomyolysis or malignant hyperpyrexia. The craniofacial abnormalities that cause difficulty with tracheal intubation may improve, worsen, or remain unchanged as craniofacial structures mature. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164087869 ER -