Macrothrombocytopenia with leukocyte inclusions in a patient with Wilson disease: a case report and literature review
Abstract Background Wilson disease (WD) is an autosomal recessive disorder caused by homozygous or compound heterozygous mutations in ATP7B. Clinical manifestations primarily involve liver and nervous system lesions, with rarely observed hematologic manifestations. Case presentation In the present c...
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Format: | Book |
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BMC,
2024-07-01T00:00:00Z.
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A1234.567 |
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