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Wilson's Disease as related to Metabolic Disorders


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

Progeria 

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...

Progeria is an extremely rare genetic condition which causes physical changes that resemble greatly accelerated aging in sufferers. It is an autosomal recessive condition that affects around 1 in 4-8 million newborns. Currently, there are approximately 35 known cases in the world with no known cure. Most children with the disease die around 13 years of age.


Wilson's Disease as related to Metabolic Disorders


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July 26, 2008


Page Updated: June 12, 2007
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