Please use this identifier to cite or link to this item: http://ddms.usim.edu.my:80/jspui/handle/123456789/15868
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dc.contributor.authorAlauddin H., Jaapar N.-A.-
dc.contributor.authorAzma R.Z., Ithnin A.-
dc.contributor.authorRazak N.-F.A., Loh C.-K.-
dc.contributor.authorAlias H., Abdul-Latiff Z.-
dc.contributor.authorOthman A-
dc.date.accessioned2018-02-13T05:18:25Z-
dc.date.available2018-02-13T05:18:25Z-
dc.date.issued2013-
dc.identifier.issn3630269-
dc.identifier.urihttp://ddms.usim.edu.my:80/jspui/handle/123456789/15868-
dc.description.abstractHb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] is a rare hemoglobin (Hb) variant due to a mutation at codon 59 of the α2- or α1-globin gene resulting in a glycine to aspartic acid substitution. Two siblings with a unique coinheritance of Hb Adana and Hb Constant Spring (Hb CS, α142, Term→Gln, TAA>CAA; HBA2: c.427 T>C) (α codon 59α/αCSα), were compared phenotypically with another two siblings carrying the Hb Adana mutation and a 3.7 kb deletion (αcodon 59α/-α3.7). Although they all had α-thalassemia intermedia (α-TI), the former were clinically more severe than the latter. The first pair of siblings presented at a much younger age than the second pair and showed lower Hb levels and significant extramedullay hemopoiesis. Another case of a hydropic fetus as a result of Hb H/Hb Adana is also described. Their clinical phenotypes and hematological parameters are all presented for comparison. © 2014 Informa Healthcare USA, Inc. All rights reserved: reproduction in whole or part not permitted.en_US
dc.language.isoenen_US
dc.publisherInforma Healthcareen_US
dc.subjectCodon 59 mutation; Hb Adana; Hb Constant Spring (Hb CS)en_US
dc.titleA case series of α-thalassemia intermedia due to compound heterozygosity for Hb Adana [HBA2: C179G>A (or HBA1); P.Gly60Asp] with other α-thalassemias in malay familiesen_US
dc.typeArticleen_US
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