Similar words: addison's disease, parkinson's disease, huntington's disease, crohn's disease, hansen's disease, hodgkin's disease, paget's disease, graves' disease. Meaning: n. a rare inherited disorder of copper metabolism; copper accumulates in the liver and then in the red blood cells and brain.
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1. However, it is difficult to detect early Wilson's disease, since caeruloplasmin activity is low in the newborn period.
2. Avoid this product if you have Wilson's disease.
3. Describe the main clinical manifestations of Wilson's disease.
4. Wilson's disease is an inherited disorder where there is excessive amounts of copper in the body.
5. Whereas in Wilson's disease livers those manipulations do not always work in the same way, and why there is a difference is very important to understand.
6. Avoid this product if you have Wilson's disease or are allergic to yeast.
7. Micronodular cirrhosis may also be seen with Wilson's disease, primary biliary cirrhosis, and hemochromatosis.
8. Metabolic diseases such as Wilson's disease, hemochromatosis, and alpha 1 - antitrypsin deficiency can lead to liver damage.
9. Cultured skin fibroblast from patients with Wilson's disease (WD) has been suggested to be used in the study of copper metabolism in WD and in the diagnosis of WD patients.
10. Portal hypertension and metabolic diseases, such as Wilson's disease and hemochromatosis, can also cause significant liver problems.
11. Conclusion:Living donor liver transplantation has been proven to be effective therapy in children with Wilson's disease for its many unsurpassed advantages.
12. Viral hepatitis (B or C) is the most common cause for macronodular cirrhosis. Wilson's disease and alpha-1-antitrypsin deficiency also can produce a macronodular cirrhosis.
13. Hemolytic anemias and psychic aberrations can be the presenting symptoms of Wilson's disease (Chapters 154 and 224).
14. So tell us Doctor, what is your perspective on the work that should be done before cell therapy can be used for treatment of Wilson's disease?
15. Methods Chinese agraphia battery (CAB), and the Xn and AgQ scores were used to identify agraphia in 35 patients with Wilson's disease.
16. The relation of the copper in the body to the disease and the important factor for clinical diagnosis; of Wilson's disease were discussed.
17. Objective To summarize experience of selection of donors of living related liver transplantation (LRLT) for Wilson's Disease.
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18. Could Edward's changing eye color be a symptom of Wilson's disease, a rare condition that causes the body to retain copper?
19. Results: MRI showed long T1, long T2 in bilateral basal ganglia and brain stem was one of the feature of Wilson's disease, another was low signals on T2WI.
20. Serum ceruloplasmin and urine copper levels were normal in the case patient: liver biopsy did not reveal copper accumulation, and there were no other findings suggestive of Wilson's disease.
21. Objective It is to explore the surgical treatment on Wilson's disease (WD) accompanied by hypersplenism and observe the adaptation and contraindication for splenectomy.
22. Objective To analyse the concentrations of 21 elements in 24 h urine of patients with Wilson's disease (WD) during penicillamine therapy.
23. Ceruloplasmin deficiency results in abnormalities of copper metabolism, as in Wilson's disease (Chapter 224).
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