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.

Keywords: deafness; diabetes mellitus; roger's syndrome; thiamine‐responsive megaloblastic anemia syndrome.