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dc.contributor.authorÇAKIR, MURAT
dc.contributor.authorİMAMOĞLU, MUSTAFA
dc.contributor.authorCANSU, AYŞEGÜL
dc.contributor.authorSag, Elif
dc.date.accessioned2022-02-18T11:18:27Z
dc.date.available2022-02-18T11:18:27Z
dc.date.issued2018
dc.identifier.citationSag E., CANSU A., İMAMOĞLU M., ÇAKIR M., "Accessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child", PEDIATRIC GASTROENTEROLOGY HEPATOLOGY & NUTRITION, cilt.21, sa.4, ss.361-364, 2018
dc.identifier.othervv_1032021
dc.identifier.otherav_e8b1961a-6f02-4b0f-9898-937c0caa37cb
dc.identifier.urihttp://hdl.handle.net/20.500.12627/180897
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/e8b1961a-6f02-4b0f-9898-937c0caa37cb/file
dc.identifier.urihttps://doi.org/10.5223/pghn.2018.21.4.361
dc.description.abstractAccessory hepatic lobe is noted as and considered a rare disease in children. It can manifest with various symptoms and complications depending on the location, volume, type and position of the disease as presented on a child. The patient presented as a 14-month-old girl who was seen with a notable hepatosplenomegaly and portal hypertension. A diagnosis was made after taking an extensive medical history, observation and radiological examinations. The formal diagnosis was a prehepatic portal hypertension associated with accessory hepatic lobe.
dc.language.isoeng
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectPediatrics
dc.subjectPediatrics, Perinatology and Child Health
dc.subjectHealth Sciences
dc.titleAccessory Hepatic Lobe: A Rare Cause of Prehepatic Portal Hypertension in a Child
dc.typeMakale
dc.relation.journalPEDIATRIC GASTROENTEROLOGY HEPATOLOGY & NUTRITION
dc.contributor.departmentKaradeniz Teknik Üniversitesi , Tıp Fakültesi , Dahili Tıp
dc.identifier.volume21
dc.identifier.issue4
dc.identifier.startpage361
dc.identifier.endpage364
dc.contributor.firstauthorID3061137


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