Prevalence of Alpha and Beta-Thalassemia Mutations Among Carriers of Thalassemia in Shadegan City, Southwest of Iran

AuthorAmin Doosti Iranien
AuthorZahra Cheraghien
AuthorSaied Bitarafen
AuthorParvin Cheraghien
AuthorSaeid Safirien
OrcidZahra Cheraghi [0000-0001-9041-559X]en
Issued Date2015-08-28en
AbstractBackground:: We aimed to investigate the alpha and beta-thalassemia mutations and assess the association of hematologic indices with mutations. Patients and Methods:: In this cross sectional study, we assessed 275 suspected thalassemia carriers. Amplification refractory mutation system-polymerase chain reaction and Gap PCR were used for detection of mutations. Results:: CD 36 - 37 (-T) and -α3.7/αα were most common mutations. Mean of corpuscular hemoglobin and corpuscular volume was less among beta-thalassemia carriers in comparison to alpha-thalassemia carriers (P = 0.001). Conclusions:: Detected mutations were different from other regions in Iran. After iron therapy, mean of corpuscular volume (MCV) was < 69 fL and mean of corpuscular hemoglobin was < 23 pg, may be classified as beta-thalassemia carriers.en
DOIhttps://doi.org/10.17795/zjrms1032en
KeywordAlpha-Thalassemiaen
KeywordBeta-Thalassemiaen
KeywordMutationen
KeywordPrevalenceen
KeywordIranen
PublisherBrieflandsen
TitlePrevalence of Alpha and Beta-Thalassemia Mutations Among Carriers of Thalassemia in Shadegan City, Southwest of Iranen
TypeBrief Reporten

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