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dc.contributorAl Nood, H.A.EN
dc.date.accessioned2014-06-17T10:25:02Z
dc.date.available2014-06-17T10:25:02Z
dc.date.issued2011EN
dc.identifier.issn1020-3397EN
dc.identifier.otherhttp://www.emro.who.int/emhj/V17/05/17_5_2011_0404_0408.pdfEN
dc.identifier.urihttp://www.who.int/iris/handle/10665/118633
dc.description404-408EN
dc.description.abstractA pilot study was conducted to determine the prevalence and haematological characteristics of the interaction between thalassaemia or/and glucose-6-phosphate dehydrogenase [‎G6PD]‎ deficiency in patients with sickle-cell disorder [‎SCD]‎ in Taiz city, Yemen, where the prevalence of sickle-cell trait [‎HbAS]‎ is 8.2%. Blood samples were collected from 31 SCD patients. Complete blood count and haemoglobin electrophoresis, G6PD activity and serum ferritin were determined. Thalassaemia was found in 6 patients [‎19.4%]‎ and G6PD deficiency [‎6 mild and 1 severe]‎ was detected in 7 patients [‎22.6%]‎ The frequency of thalassaemia and/or G6PD deficiency with SCD was high and this may have an effect on the seventy of the clinical course of SCD in Taiz. The study should be repeated with DNA analysis to define the nature of the globin gene defect and to clarify its role in the severity of SCDEN
dc.language.isoenEN
dc.subjectThalassemiaEN
dc.subjectGlucosephosphate Dehydrogenase DeficiencyEN
dc.subjectPrevalenceEN
dc.subjectComorbidityEN
dc.subject.meshAnemia, Sickle CellEN
dc.titleThalassaemia and glucose-6-phosphate dehydrogenase deficiency in sickle-cell disorder patients in Taiz, YemenEN
dc.relation.ispartofjournalEMHJ - Eastern Mediterranean Health Journal, 17 (‎5)‎, 404-408, 2011


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