Rett syndrome and anesthetic management; [Rett sendromu ve anestezi yönetimi]

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dc.contributor.authorÇevikkalp E.
dc.contributor.authorGül Hayran G.
dc.contributor.authorTezcan Keleş G.
dc.date.accessioned2024-07-22T08:11:10Z
dc.date.available2024-07-22T08:11:10Z
dc.date.issued2017
dc.description.abstractRett 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.
dc.identifier.issn13000578
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/15544
dc.language.isoTurkish
dc.publisherAnestezi Dergisi
dc.subjectanesthetic agent
dc.subjectmethyl CpG binding protein 2
dc.subjectapnea
dc.subjectArticle
dc.subjectcachexia
dc.subjectEEG abnormality
dc.subjectgene mutation
dc.subjectheart disease
dc.subjecthuman
dc.subjectmental deficiency
dc.subjectmusculoskeletal disease
dc.subjectQT prolongation
dc.subjectrespiratory tract disease
dc.subjectRett syndrome
dc.subjectscoliosis
dc.subjectseizure
dc.titleRett syndrome and anesthetic management; [Rett sendromu ve anestezi yönetimi]
dc.typeArticle

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