Epidemiology, diagnosis, and treatment of Wilson's disease
- PMID: 29259852
- PMCID: PMC5735277
- DOI: 10.5582/irdr.2017.01057
Epidemiology, diagnosis, and treatment of Wilson's disease
Abstract
Wilson's disease (WD) is an autosomal recessive disease caused by a mutation of the ATP7B gene, resulting in abnormal copper metabolism. The major clinical features of WD include liver disease, neurological disorders, K-F rings, and osteoporosis. The prevalence of WD in China is higher than that in Western countries. Early diagnosis and lifelong treatment will lead to better outcomes. Drugs such as sodium dimercaptosuccinate (Na-DMPS), Zn, and Gandou Decoction can be used to treat WD. Some studies have shown that the combination of traditional Chinese medicine and Western medicine is the best approach to treating WD. In order to identify better treatments, this article describes the specific clinical symptoms of Wilson's disease, its diagnosis, and treatment options.
Keywords: D-PCA; Kayser-Fleischer rings; Wilson's disease.
References
-
- Hahn SH. Population screening for Wilson's disease. Ann N Y Acad Sci. 2014; 1315:64-69. - PubMed
-
- Cheng YL. Hepatolenticular degeneration (pseudosclerosis, progressive lenticular degeneration and torsion spasm) review of literature and report of two cases. Chin Med J. 1932; 46:347-364.
-
- Li WJ, Wang JF, Wang XP. Wilson's disease: Update on integrated Chinese and Western medicine. Chin J Integr Med. 2013; 19:233-240. - PubMed
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