Congenital dyserythropoietic anemia masquerading as hereditary spherocytosis
Background: Congenital dyserythropoietic anemias (CDA) type II is a rare hereditary chronic hemolytic anemia due to a defect in the SEC23B gene which shows varying degrees of ineffective erythropoiesis and is often misdiagnosed as a red blood cell (RBC) membranopathy or enzymopathy. Case report: A f...
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Format: | Book |
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Elsevier,
2024-09-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |