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Wilson's Disease as related to Ectodermal dysplasia


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Copper storage disease; Hepatolenticular Degeneration; Hepatolenticular degeneration syndrome; WD - Wilson's disease; Wi... 

 

Wilson's disease is an inherited disorder in which excessive amounts of copper accumulate in the body. Although the accumulation of copper begins at birth, symptoms of the disorder appear later in life, between the ages of 6 and 40. The primary consequence for approximately 40 percent of patients with Wilson's is liver disease. In other patients the first symptoms are either neurological or psychiatric or both, and include tremor, rigidity, drooling, difficulty with speech, abrupt personality ch...


Wilson's Disease as related to Ectodermal dysplasia


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November 22, 2009


Page Updated: January 17, 2009
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