Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease
Copyright © 2017 Wolters Kluwer Health, Inc. All rights reserved. Hereditary elliptocytosis is an inherited red blood cell membrane disorder characterized by typical peripheral blood smear findings of elliptocytes or rod-like red blood cells. Hemoglobin H disease is a form of α-thalassemia disease r...
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th-cmuir.6653943832-577892018-09-05T03:49:48Z Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease Pimlak Charoenkwan Rungrote Natesirinilkul Worawut Choeyprasert Natchanon Kulsumritpon Orapan Sangiamporn Medicine Copyright © 2017 Wolters Kluwer Health, Inc. All rights reserved. Hereditary elliptocytosis is an inherited red blood cell membrane disorder characterized by typical peripheral blood smear findings of elliptocytes or rod-like red blood cells. Hemoglobin H disease is a form of α-thalassemia disease resulting in mild to moderate hemolytic anemia. The authors report 1 case of a girl who was diagnosed with oculo-auriculo-vertebral spectrum and a coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease. She had moderate, non-transfusion-dependent anemia. The red blood cells showed marked poikilocytosis and fragmentation. The parents were α-thalassemia carriers and the father had the typical red blood cell morphology of common hereditary elliptocytosis. 2018-09-05T03:49:48Z 2018-09-05T03:49:48Z 2017-01-01 Journal 15363678 10774114 2-s2.0-85008334872 10.1097/MPH.0000000000000750 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85008334872&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/57789 |
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Medicine Pimlak Charoenkwan Rungrote Natesirinilkul Worawut Choeyprasert Natchanon Kulsumritpon Orapan Sangiamporn Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease |
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Copyright © 2017 Wolters Kluwer Health, Inc. All rights reserved. Hereditary elliptocytosis is an inherited red blood cell membrane disorder characterized by typical peripheral blood smear findings of elliptocytes or rod-like red blood cells. Hemoglobin H disease is a form of α-thalassemia disease resulting in mild to moderate hemolytic anemia. The authors report 1 case of a girl who was diagnosed with oculo-auriculo-vertebral spectrum and a coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease. She had moderate, non-transfusion-dependent anemia. The red blood cells showed marked poikilocytosis and fragmentation. The parents were α-thalassemia carriers and the father had the typical red blood cell morphology of common hereditary elliptocytosis. |
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Journal |
author |
Pimlak Charoenkwan Rungrote Natesirinilkul Worawut Choeyprasert Natchanon Kulsumritpon Orapan Sangiamporn |
author_facet |
Pimlak Charoenkwan Rungrote Natesirinilkul Worawut Choeyprasert Natchanon Kulsumritpon Orapan Sangiamporn |
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Pimlak Charoenkwan |
title |
Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease |
title_short |
Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease |
title_full |
Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease |
title_fullStr |
Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease |
title_full_unstemmed |
Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease |
title_sort |
coinheritance of hereditary elliptocytosis and deletional hemoglobin h disease |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85008334872&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/57789 |
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