Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease

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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Main Authors: Charoenkwan P., Natesirinilkul R., Choeyprasert W., Kulsumritpon N., Sangiamporn O.
Format: Journal
Published: 2017
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85008334872&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40888
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-408882017-09-28T04:14:20Z Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease Charoenkwan P. Natesirinilkul R. Choeyprasert W. Kulsumritpon N. Sangiamporn O. 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. 2017-09-28T04:14:20Z 2017-09-28T04:14:20Z 2017-01-01 Journal 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/6653943832/40888
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description 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.
format Journal
author Charoenkwan P.
Natesirinilkul R.
Choeyprasert W.
Kulsumritpon N.
Sangiamporn O.
spellingShingle Charoenkwan P.
Natesirinilkul R.
Choeyprasert W.
Kulsumritpon N.
Sangiamporn O.
Coinheritance of hereditary elliptocytosis and deletional hemoglobin H disease
author_facet Charoenkwan P.
Natesirinilkul R.
Choeyprasert W.
Kulsumritpon N.
Sangiamporn O.
author_sort Charoenkwan P.
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
publishDate 2017
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85008334872&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/40888
_version_ 1681421900616564736

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