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dc.contributor.authorKaya, Guner
dc.contributor.authorKendigelen, Pinar
dc.contributor.authorTutuncu, Ayse Cigdem
dc.date.accessioned2021-03-05T18:19:51Z
dc.date.available2021-03-05T18:19:51Z
dc.date.issued2017
dc.identifier.citationTutuncu A. C. , Kendigelen P., Kaya G., "Anesthetic Management of Leigh Syndrome", BEZMIALEM SCIENCE, cilt.5, ss.84-85, 2017
dc.identifier.othervv_1032021
dc.identifier.otherav_c9d7d4e5-af66-4638-b036-decb6959450e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/133727
dc.identifier.urihttps://doi.org/10.14235/bs.2016.855
dc.description.abstractLeigh syndrome is an extremely rare disorder in infants and children. It is characterized by a progressive neurodegenerative course with subacute necrotizing encephalomyelopathy, and it presents with developmental delay, seizures, dysarthria, ataxia, and myopathy. We present a patient with Leigh syndrome who required general anesthesia for percutaneous endoscopic gastrostomy. The respiratory, cardiac, and renal system functions should be very carefully evaluated in the peroperative period. The use of long-acting opioids and neuromuscular agents increases postoperative respiratory complications related to neuromuscular myopathy. Considering that lactic acidosis can develop in the perioperative period, it is recommended to give pre-perioperative fluids with dextrose.
dc.language.isoeng
dc.subjectTıp
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectTIP, GENEL & İÇECEK
dc.titleAnesthetic Management of Leigh Syndrome
dc.typeMakale
dc.relation.journalBEZMIALEM SCIENCE
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume5
dc.identifier.issue2
dc.identifier.startpage84
dc.identifier.endpage85
dc.contributor.firstauthorID241772


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