Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Keimyung Medical Journal ; : 204-208, 2015.
Article in Korean | WPRIM | ID: wpr-12450

ABSTRACT

Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu disease, is a rare autosomal dominant vascular disorder involving arteriovenous malformation. HHT is characterized by recurrent epistaxis, cutaneous telangiectasia, and visceral arteriovenous malformations. Hepatic arteriovenous malformation can lead to high output heart failure. We report a case of hereditary hemorrhagic telangiectasia patient who complained dyspnea and edema on both lower extremity.


Subject(s)
Humans , Arteriovenous Malformations , Dyspnea , Edema , Epistaxis , Heart Failure , Heart , Lower Extremity , Telangiectasia, Hereditary Hemorrhagic , Telangiectasis
SELECTION OF CITATIONS
SEARCH DETAIL