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Inositol and its most abundant metabolite myo-inositol have a protective effect on the thyroid gland by improving TSH signaling and proinflammatory cytokine suppression [10]

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Most patients have no family history of the condition.[16] People with only one abnormal gene are called carriers (heterozygotes) and may have mild, but medically insignificant, abnormalities of copper metabolism.[20] Wilson’s disease is the most common of a group of hereditary diseases that cause copper overload in the liver