Minimal encephalopathy in hereditary hemorrhagic telangiectasia patients with portosystemic vascular malformations

Minimal encephalopathy in hereditary hemorrhagic telangiectasia patients with portosystemic vascular malformations

Abstract Background Hereditary hemorrhagic telangiectasia (HHT) is characterized by telangiectasia and larger vascular malformations. Liver malformations are the most frequent visceral involvement including the presence of portosystemic malformations (PSM) that can cause hepatic encephalopathy. Mini...

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Main Authors: B. Villanueva, A. Cañabate, R. Torres-Iglesias, P. Cerdà, E. Gamundí, Q. Ordi, E. Alba, L. A. Sanz-Astier, A. Iriarte, J. Ribas, J. Castellote, X. Pintó, A. Riera-Mestre
Format: Article
Language:English
Published: BMC 2024-12-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Hereditary hemorrhagic telangiectasia
Hepatic encephalopathy
Rare diseases
Portosystemic malformations
Online Access:https://doi.org/10.1186/s13023-024-03493-3
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https://doi.org/10.1186/s13023-024-03493-3

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