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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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Vydáno v:Indian J Gastroenterol
Hlavní autoři: Amalnath, S. Deepak, Sargolzaeiaval, Forough, Oshima, Junko, Baskar, Dipti
Médium: Artigo
Jazyk:Inglês
Vydáno: 2017
Témata:
On-line přístup: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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