Wilson's disease causes: Difference between revisions
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Line 10: | Line 10: | ||
*Genetic mutations: | *Genetic mutations: | ||
**ATP7B ''gene'' | **ATP7B ''gene'' | ||
*Impairment mechanisms which lead to Wilson's disease include the following: | |||
**Imapired copper incorporation in ceruloplasmin production | |||
**Copper accumulation in the liver | |||
**Extrahepatic copper accumulation | |||
==References== | ==References== |
Revision as of 14:48, 28 December 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]
Overview
Wilson's disease is caused by ATP7B gene mutation and impairement of copper transportation.
Causes
- Wilson's disease is caused mainly by mutations in the genes responsible for copper transport.
- Genetic mutations:
- ATP7B gene
- Impairment mechanisms which lead to Wilson's disease include the following:
- Imapired copper incorporation in ceruloplasmin production
- Copper accumulation in the liver
- Extrahepatic copper accumulation