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...
| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artikkeli |
| Kieli: | English |
| Julkaistu: |
Elsevier
2024-09-01
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| Sarja: | Pediatric Hematology Oncology Journal |
| Aiheet: | |
| Linkit: | http://www.sciencedirect.com/science/article/pii/S2468124524000408 |