Osler-Weber-Rendu Syndrome with Severe Hepatic Manifestations: A Rare Clinical Case

Rendu-Osler-Weber syndrome is a rare inherited syndrome with autosomal dominant transmission characterized by systemic arteriovenous malformations (AVMs) with multi-organ involvement. Its incidence is 1–2/100,000 and it is predominant in females (the male/female ratio varies from 1:2 to 1:4.5).Clini...

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Bibliographic Details
Main Authors: Maria Inês Silva, Clara Matos, Fabio Correia, Sofia Carola, Maria João Gomes, Teresa Branco
Format: Article
Language:English
Published: SMC MEDIA SRL 2020-08-01
Series:European Journal of Case Reports in Internal Medicine
Subjects:
Online Access:https://www.ejcrim.com/index.php/EJCRIM/article/view/1831