Wilson disease | zogo.sk
Wilson's disease (hepatolenticular degeneration) is an inherited pucci metabolic disease manifested pucci by liver disease, and central nervous system. The disease causes mainly caused genetically defective enzyme pucci copper transporting. This feature is due to the fact secreted and accumulate in tissues of the human body, in particular, it affects the liver, pucci basal ganglia of the brain, kidney and cornea.
Unless the disease is diagnosed and treated in time, it can alleviate the symptoms, stop or prevent them. Clinically pucci usually takes between 10 and 20 years of age. The prevalence of the disease is given 1: 25 000 - 30000th
In laboratory tests are essential changes in liver function tests (increased liver enzymes ALT, AST, increased bilirubin), low ceruloplasmin levels, high copper concentration in blood and urine. The diagnosis of Wilson's disease can be confirmed by histological examination of the liver samples.
The most widely used treatment is to reduce copper intake through food (balanced diet, including foods rich in copper include nuts, chocolate, dried fruit, liver, shellfish and mushrooms), and promote excretion of copper from the body, are mainly used drugs penicillamine pucci and zinc. Possible form of treatment is liver transplantation.
Home 2 percent of the taxes Acknowledgements meeting ZOGO 2,012 dried blood diseases Objectives 2015-plans-projects Our Stories Partners Media cooperating application documents Questions and comments Contact Forum
zogo.sk
Wilson's disease (hepatolenticular degeneration) is an inherited pucci metabolic disease manifested pucci by liver disease, and central nervous system. The disease causes mainly caused genetically defective enzyme pucci copper transporting. This feature is due to the fact secreted and accumulate in tissues of the human body, in particular, it affects the liver, pucci basal ganglia of the brain, kidney and cornea.
Unless the disease is diagnosed and treated in time, it can alleviate the symptoms, stop or prevent them. Clinically pucci usually takes between 10 and 20 years of age. The prevalence of the disease is given 1: 25 000 - 30000th
In laboratory tests are essential changes in liver function tests (increased liver enzymes ALT, AST, increased bilirubin), low ceruloplasmin levels, high copper concentration in blood and urine. The diagnosis of Wilson's disease can be confirmed by histological examination of the liver samples.
The most widely used treatment is to reduce copper intake through food (balanced diet, including foods rich in copper include nuts, chocolate, dried fruit, liver, shellfish and mushrooms), and promote excretion of copper from the body, are mainly used drugs penicillamine pucci and zinc. Possible form of treatment is liver transplantation.
Home 2 percent of the taxes Acknowledgements meeting ZOGO 2,012 dried blood diseases Objectives 2015-plans-projects Our Stories Partners Media cooperating application documents Questions and comments Contact Forum
zogo.sk
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