eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | wilson disease |
| Comorbidity | C0023895|liver diseases |
| Sentences | 4 |
| PubMedID- 20535024 | Conclusions: patients with concurrent liver diseases were diagnosed with wilson disease at significantly older ages, presented with more liver cirrhosis, and showed greater mortality. |
| PubMedID- 24972800 | Search for rare liver diseases: the case of glycosylation defects mimicking wilson disease. |
| PubMedID- 23180946 | Conclusion: we suggest that screening for celiac disease may be beneficial not only in patients with associated liver diseases, but also in patients with wilson's disease. |
| PubMedID- 25717050 | Children were considered to have dili if they met the following criteria:16–18 a clinical suspicion of drug-induced hepatotoxicity, as defined as recent onset abnormalities in liver tests, such as rise in serum total bilirubin (tb) of at least 2 mg/dl, and/or alanine aminotransferase (alt) or aspartate aminotransferase (ast) >3 times the upper limit of normal (uln), or rise in alkaline phosphatase (alp) >2 times the uln with any rise in tb or alt or ast; exclusion of viral hepatitis a to e, hepatitis caused by nonhepatotropic virus, autoimmune liver disease, hepatolenticular degeneration, and other causes of liver diseases; and based on the roussel uclaf causality assessment method (rucam), highly probable (>8), probable (6 to 8), or possible (3 to 5) are considered drug-induced liver injury. |
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