2026-06-27T12:04:07Z https://meral.edu.mm/oai

oai:meral.edu.mm:recid/3180 2021-12-13T05:41:28Z 1582963366982:1596631630241 user-um1

Hyperhemolysis with hemoglobin H disease Sein Win Thida Aung June Myo Aung Kyaw Thet Aye Swe Zin Oo Htun Lwin Nyein Rai Mra <p>Hyperhemolysis syndrome is one of serious and potentially life-threatening complications of red blood cell transfusion, and is well described in sickle cell disease as well as in thalassaemias and other anaemias. It also is a great diagnostic and management challenge to laboratory scientists and attending physician taking care of patients with such kinds of diseases. A Myanmar patient with hemoglobin H disease presenting with acute hyperhemolysis syndrome was diagnosed timely and successfully treated with intravenous immunoglobulin (IV Ig) and methylprednisolone. A high index of suspicion allowing early diagnosis and prompt management can save lives of patients with hyperhemolysis syndrome.</p> 2017-10-18 http://hdl.handle.net/20.500.12678/0000003180 https://meral.edu.mm/records/3180