Anesthetic management in progressive familial intrahepatic cholestasis type i (Byler Disease)

dc.contributor.authorDemirel, Ismail
dc.contributor.authorBolat, Esef
dc.contributor.authorAltun, Aysun Yildiz
dc.contributor.authorAtici, Erkan
dc.contributor.authorTartar, Tugay
dc.date.accessioned2026-08-12T16:12:50Z
dc.date.issued2018
dc.departmentFırat Üniversitesi
dc.description.abstractProgressive familial intrahepatic cholestasis (PFIC) or Byler disease is one of the most common forms of intrahepatic cholestasis of metabolic and genetic origin. It's an autosomal recessive disease and appears in the first 6 months of life with intrahepatic cholestasis and progressive fibrosis resulting with cirrhosis. Patients usually die because of hepatic deficiency before adolescant period. In this study we would like to report about an eight year old girl diagnosed with Byler disease since 1,5 year of age planned for laparoscopic cholecystectomy due to calculous cholecystitis under general anasthesia. This case report describes the anesthetic features of a patient with Byler's disease in which anesthetic agents with no or minimal hepatotoxic effect should be used to avoid deterioration of liver function. © 2018 Anestezi Dergisi. All rights reserved.
dc.identifier.endpage39
dc.identifier.issn1300-0578
dc.identifier.issue1
dc.identifier.scopus2-s2.0-85048719649
dc.identifier.scopusqualityQ4
dc.identifier.startpage36
dc.identifier.urihttps://hdl.handle.net/11508/42694
dc.identifier.volume26
dc.indekslendigikaynakScopus
dc.language.isotr
dc.publisherAnestezi Dergisi
dc.relation.ispartofAnestezi Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20260511
dc.subjectAnesthesia management; Byler disease; Laparoscopic cholecystectomy
dc.titleAnesthetic management in progressive familial intrahepatic cholestasis type i (Byler Disease)
dc.typeArticle

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