Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/54707
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dc.contributor.authorKasemsri Srisupunditen_US
dc.contributor.authorPimlak Charoenkwanen_US
dc.contributor.authorKuntharee Traisrisilpen_US
dc.contributor.authorTheera Tongsongen_US
dc.date.accessioned2018-09-04T10:21:20Z-
dc.date.available2018-09-04T10:21:20Z-
dc.date.issued2015-07-27en_US
dc.identifier.issn1757790Xen_US
dc.identifier.other2-s2.0-84941312985en_US
dc.identifier.other10.1136/bcr-2014-208196en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84941312985&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/54707-
dc.description.abstractThe case presented here is an example of hereditary red blood cell membrane defect with a co-inherited haemoglobin Constant Spring. This case is of an anaemic fetus that presented with isolated ascites at 18 weeks of gestation. Fetal blood analysis revealed abnormal shaped red blood cells. The same pattern of red blood cell morphology was also seen on paternal peripheral blood smear. Intrauterine blood transfusions were given twice to correct fetal anaemia. The fetus showed a good response to the transfusions and was delivered at term with mild anaemia and did not need blood transfusion after birth. This report describes a natural course of red blood cell membrane defect with co-inherited haemoglobin Constant Spring, indicating that the course of disease was more severe during fetal life. Intrauterine transfusion supported the transition of the fetus through the critical period in utero to a healthier life after birth.en_US
dc.subjectMedicineen_US
dc.titleFetal anaemia from red blood cell membrane defect and co-inherited haemoglobin Constant Springen_US
dc.typeJournalen_US
article.title.sourcetitleBMJ Case Reportsen_US
article.volume2015en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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