{"created":"2020-08-30T20:06:08.664938+00:00","id":3180,"links":{},"metadata":{"_buckets":{"deposit":"54ce635a-5b9a-4cfa-8d57-e7878c948135"},"_deposit":{"id":"3180","owners":[],"pid":{"revision_id":0,"type":"recid","value":"3180"},"status":"published"},"_oai":{"id":"oai:meral.edu.mm:recid/3180","sets":["1582963366982:1596631630241"]},"communities":["um1"],"item_1583103067471":{"attribute_name":"Title","attribute_value_mlt":[{"subitem_1551255647225":"Hyperhemolysis with hemoglobin H disease","subitem_1551255648112":""}]},"item_1583103085720":{"attribute_name":"Description","attribute_value_mlt":[{"interim":"

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.

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