Dyserythropoiesis and myelodysplasia in thiamine‐responsive megaloblastic anemia syndrome

Abstract

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