75세 여자 환자에서 재발성 간성뇌증으로 발현한 유전성 출혈성 혈관 확장증

Osler-Weber-Rendu disease is a rare autosomal dominant disorder of fibrovascular tissues, characterized by a classic triad of mucocutaneous telangiectasias, recurrent hemorrhages, and a familial occurrence. Portosystemic encephalopathy in a patient with Osler-Weber-Rendu disease is rare, but we expe...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	The Korean journal of gastroenterology 2015-01, Vol.65 (1), p.57
Hauptverfasser:	하정훈, Jung Hoon Ha, 손병관, Byoung Kwan Son, 안상봉, Sang Bong Ahn, 조영관, Young Kwan Jo, 김성환, Seong Hwan Kim, 조윤주, Yun Ju Jo, 박영숙, Young Sook Park, 정윤영, Yoon Young Jung
Format:	Artikel
Sprache:	kor
Schlagworte:	Hepatic encephalopathy Hereditary hemorrhagic telangiectasia
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!