Gilbert syndrome in patients with inherited hemolytic anemia modifies the clinical phenotype
Gilbert syndrome is a benign condition due to UGT1A1 mutations frequently resulting in mild, indirect hyperbilirubinemia. Inherited hemolytic anemias often present with hyperbilirubinemia and hepatosplenomegaly. Over the years, there have been multiple case reports/series in which the extent of unco...
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| Main Authors: | , |
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| Format: | Book |
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Elsevier,
2024-06-01T00:00:00Z.
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Internet
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |