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Uncommon cause of cirrhosis—A case of Werner syndrome with a novel WRN mutation
Werner syndrome is a rare progeroid syndrome caused by the WRN gene mutation. It is characterized by a general appearance of premature aging, diabetes mellitus, and atherosclerosis, and an increased risk of malignancies. We report a patient who presented with hematemesis due to cirrhosis of liver an...
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| Publicado no: | Indian J Gastroenterol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5648602/ https://ncbi.nlm.nih.gov/pubmed/28795391 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12664-017-0781-1 |
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