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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Intern Med |
|---|---|
| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
The Japanese Society of Internal Medicine
2020
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8188034/ https://ncbi.nlm.nih.gov/pubmed/33361674 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2169/internalmedicine.5670-20 |
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