Çevikkalp E.Gül Hayran G.Tezcan Keleş G.2024-07-222024-07-22201713000578http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/15544Rett syndrome is a developmental and neurological disease characterized by defective X and is caused by mutations in the gene MECP2 coded chromosomes. It is a central involvement diesase that starts in the early developmental years, together along with EEG abnormalities, seizures, mental retardation. Orthopedic, respiratory and cardiac problems can also be seen. Prolonged QT, scoliosis, apnea, cachexia is common in children with this syndrome and requires significant anesthesia care and attention. In this case, we emphasized the anesthetic management of a Rett Syndrome child, its possible risks and problems.Turkishanesthetic agentmethyl CpG binding protein 2apneaArticlecachexiaEEG abnormalitygene mutationheart diseasehumanmental deficiencymusculoskeletal diseaseQT prolongationrespiratory tract diseaseRett syndromescoliosisseizureArticle