Hereditary Hemorrhagic Telangiectasia Induced Portosystemic Encephalopathy: A Case Report and Literature Review

Hereditary hemorrhagic telangiectasia (HHT) is a rare disorder characterized by telangiectasias and arteriovenous malformations (AVMs), which can involve multiple organ systems. Although hepatic involvement is common, the development of portosystemic encephalopathy is extremely rare. We herein repor...

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Detalles Bibliográficos
Autores principales: Kawabata, Hiroyuki, Hamada, Yasuhiko, Hattori, Aiji, Tanaka, Kyosuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188034/
https://www.ncbi.nlm.nih.gov/pubmed/33361674
http://dx.doi.org/10.2169/internalmedicine.5670-20

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8188034/
https://www.ncbi.nlm.nih.gov/pubmed/33361674
http://dx.doi.org/10.2169/internalmedicine.5670-20

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