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dc.contributor.authorChane Choed-Amphaien_US
dc.contributor.authorArunee Phusuaen_US
dc.contributor.authorChupong Ittiwuten_US
dc.contributor.authorPimlak Charoenkwanen_US
dc.contributor.authorKanya Suphapeetipornen_US
dc.contributor.authorVorasuk Shotelersuken_US
dc.date.accessioned2022-10-16T07:22:23Z-
dc.date.available2022-10-16T07:22:23Z-
dc.date.issued2021-07-01en_US
dc.identifier.issn15363678en_US
dc.identifier.issn10774114en_US
dc.identifier.other2-s2.0-85109037002en_US
dc.identifier.other10.1097/MPH.0000000000001937en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85109037002&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/77076-
dc.description.abstractHemoglobin (Hb) H/Constant Spring disease is a common nondeletional Hb H disease, typically causing a more severe phenotype than the deletional Hb H disease counterpart. Hb Tak, resulting from a dinucleotide insertion (+AC) at codon 146 of beta-globin gene, has an increased oxygen affinity and usually presents with polycythemia. We studied a case of a 4-year-old Thai boy with a severe, early-onset anemia. To our knowledge, he is the first reported patient with Hb H/Constant Spring disease and heterozygous Hb Tak. Trio-whole-exome sequencing does not identify other genetic variants that may contribute to the severity of anemia. The observation suggests that coinherited Hb H/Constant Spring and heterozygous Hb Tak lead to severe hemolytic anemia.en_US
dc.subjectMedicineen_US
dc.titleCoinherited Hemoglobin H/Constant Spring Disease and Heterozygous Hemoglobin Tak Causing Severe Hemolytic Anemia in a Thai Boyen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Pediatric Hematology/Oncologyen_US
article.volume43en_US
article.stream.affiliationsChulalongkorn Universityen_US
article.stream.affiliationsKing Chulalongkorn Memorial Hospitalen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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