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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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2024-09-01
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| Col·lecció: | Pediatric Hematology Oncology Journal |
| Matèries: | |
| Accés en línia: | http://www.sciencedirect.com/science/article/pii/S2468124524000408 |
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