Dyserythropoiesis and myelodysplasia in thiamine‐responsive megaloblastic anemia syndrome
Abstract The case of thiamine‐responsive megaloblastic anemia (TRMA) presented here speculates the need early diagnosis, continuous monitoring, follow‐up, and regulated treatment plan for the patients. Complications and systemic manifestations are likely to enhance in otherwise circumstances.
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| Hauptverfasser: | , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Wiley
2020-06-01
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| Schriftenreihe: | Clinical Case Reports |
| Schlagworte: | |
| Online-Zugang: | https://doi.org/10.1002/ccr3.2791 |
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