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Dyserythropoiesis and myelodysplasia in thiamine-responsive megaloblastic anemia syndrome.

Mojgan Faraji-GoodarziFariba TarhaniNadereh Taee
Published in: Clinical case reports (2020)
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.
Keyphrases
  • end stage renal disease
  • chronic kidney disease
  • ejection fraction
  • cancer therapy
  • peritoneal dialysis
  • iron deficiency
  • transcription factor
  • drug delivery
  • drug induced