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dc.contributor.authorSitthichai Panyasaien_US
dc.contributor.authorPollawat Thongsuken_US
dc.contributor.authorSakorn Pornpraserten_US
dc.date.accessioned2018-09-05T02:53:23Z-
dc.date.available2018-09-05T02:53:23Z-
dc.date.issued2016-03-03en_US
dc.identifier.issn1532432Xen_US
dc.identifier.issn03630269en_US
dc.identifier.other2-s2.0-84959554056en_US
dc.identifier.other10.3109/03630269.2016.1138126en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84959554056&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/55232-
dc.description.abstract© 2016 Taylor & Francis. Hb Agenogi [β90(F6)Glu→Lys (GAG>AAG) HBB: c.271G>A)] is a very rare β-globin chain variant. We report for the first time this hemoglobinopathy in a pregnant 20-year-old Thai woman. She was seen by an obstetrician at her 14th week of gestation. She was pale and had an inflammatory lesion of her lower left leg. The hemoglobin (Hb) analysis by high performance liquid chromatography (HPLC) and low pressure liquid chromatography (LPLC) showed a peak of abnormal Hb at the C window. On capillary electrophoresis (CE), the abnormal Hb peak was observed at electrophoretic zone 4 that corresponded to the Hb E (HBB: c.79G>A) peak. Direct DNA sequencing revealed a GAG>AAG mutation at codon 90 of the β-globin gene. Thus, even though Hb Agenogi is very rare, it can be found in Thai people. The knowledge and understanding of this hemoglobinopathy will be used to assist in diagnosis, management and counseling for patients.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleHb Agenogi [β 90(F6)Glu→Lys (G AG> A AG) HBB: C.271G>A)] in a Pregnant Thai Womanen_US
dc.typeJournalen_US
article.title.sourcetitleHemoglobinen_US
article.volume40en_US
article.stream.affiliationsUniversity of Phayaoen_US
article.stream.affiliationsChiangrai Prachanukroh Hospitalen_US
article.stream.affiliationsChiang Mai Universityen_US
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