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ウィルソン病
先天性遺伝子オレゴン, 肝臓胆嚢と胆管, neurology
[慢性]
異常歩行, 貧しい人々の調整, 首の痛み, yellow color of skin and eyes
Wilson's disease or hepatolenticular degeneration is an autosomal recessive hereditary disease, with an incidence of about 1 in 30,000 in most parts of the world and a male preponderance. Its main feature is accumulation of copper in tissues, which manifests itself with neurological symptoms and liver disease.
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