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Updated: Apr 21, 2026

Detection of Residual Donor Erythroid Progenitor Cells after Hematopoietic Stem Cell Transplantation for Patients with Hemoglobinopathies
Published on: September 6, 2017
Remission of microangiopathy in transplanted thalassemic child
Priya Marwah1, Rajpreet Soni1, Lawrence Faulkner2
1South East Asia Institute for Thalassemia, Prem Niketan Hospital, Ashram Marg, Near Durgapura Byepass, Jaipur, 302016 India.
Abstract:
Transplant associated thrombotic microangiopathy is a severe complication of Hematopoeitic stem cell transplantation. Although there is agreement in terms of diagnostic criteria, treatment options are not clarified yet. We present a patient aged 2.6 years who developed transplant associated thrombotic microangiopathy after allogeneic bone marrow transplantation and to discuss both risk factors and possible spontaneous remission of transplant associated thrombotic microangiopathy.
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