| Literature DB >> 24440034 |
Cara M Bevinetto1, Alan D Kaye2.
Abstract
Angelman syndrome arises by one of 4 genetic mechanisms. Patients often have craniofacial abnormalities, vagal hypertonia, skeletal muscle atrophy or underdevelopment, a history of seizure disorders, and pharmacodynamic unpredictability. Its pathogenesis, clinical manifestations, diagnosis and treatment options, and perioperative anesthetic considerations are presented.Entities:
Keywords: Anesthesia; Angelman syndrome; Craniofacial abnormalities; Vagal hypertonia
Mesh:
Year: 2014 PMID: 24440034 DOI: 10.1016/j.jclinane.2013.07.015
Source DB: PubMed Journal: J Clin Anesth ISSN: 0952-8180 Impact factor: 9.452