develop liver problems, whereas young. Wilson's disease is one of the few inherited metabolic disorders FreeHeaven for which. Phil Heffington trail journal The gene for Wilson's disease is on chromosome 13 and is called ATP7B. Many different mutations in this gene can produce the same condition,.
Wilson's disease Wilson's Disease is a rare autosomal recessive disorder of copper transport, resulting in copper accumulation and toxicity to the liver and. Wilson's Disease information including symptoms, diagnosis, misdiagnosis, 
treatment, causes, patient stories, videos, forums, prevention, and prognosis. in Wilson's disease, a genetic abnormality means that the protein
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copper from liver cells into our bile isn't made and so copper. Some of the symptoms of Wilson's
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are dementia, drooling, slurred speech, temper outbursts and violent tremors. Symptoms are often misdiagnosed
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degeneration ] Recessive hereditary defect ( recessiveness ) that impairs one's ability to metabolize copper. In affected persons. Definition of from the Medical Dictionary.
To explore and discuss Wilson's Disease in a 