hepatolenticular degeneration/oxalis tuberosa

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A case report: Co-occurrence of Wilson disease and oculocutaneous albinism in a Chinese patient.

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Both Wilson disease (WD) and Oculocutaneous Albinism (OCA) are rare autosomal recessive disorders that are caused by mutations on chromosome 13 and chromosome 11, respectively. Here, we report on a patient with coexisting WD and OCA, initially presenting episodes of

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Herbal & Natural Medicine

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