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Dyserythropoiesis and myelodysplasia in thiamine‐responsive megaloblastic anemia syndrome
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.
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303871/ https://www.ncbi.nlm.nih.gov/pubmed/32577249 http://dx.doi.org/10.1002/ccr3.2791 |