- Clinical Characteristics of Pediatric Thalassemia in Korea: A Single Institute Experience
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Hong CR, Kang HJ, Lee JW, Kim H, Kim NH, Park KD, Park JD, Seong MW, Park SS, Shin HY, Ahn HS
- KMID: 1777663
- J Korean Med Sci.
- 2013 Nov;28(11):1645-1649.
- doi: 10.3346/jkms.2013.28.11.1645
Few literatures have elaborated on the clinical characteristics of children with thalassemia from low-prevalence areas. A retrospective analysis was conducted on children genetically confirmed with thalassemia at Seoul National University... -
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- A Korean Family with Thalassemia Intermedia due to Co-inheritance of Triplicated alpha-Globin Genes (alphaalpha/alphaalphaalphaanti3.7) and beta-Thalassemia Trait (IVSII-1 G -> A)
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Han JY, Kim TG, Kim KH, Kim IH, Lee EY, Cho GJ, Ren ZR, Huang SZ, Zeng YT, Rodgers GP
- KMID: 2083384
- Korean J Hematol.
- 1999 May;34(2):338-343.
We report a Korean family in which the interaction of a triplicated alpha-globin locus and a heterozygous beta-thalassemia gives rise to a clinical phenotype of thalassemia intermedia. The propositus, a... -
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- A Case of Heterozygous alpha(+)-Thalassemia Diagnosed in a Korean Family by Using Multiplex Ligation-Dependent Probe Amplification
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Oh AC, Lee JK, Hong YJ, Hong SI, Yang SH, Park CH, Kim HJ, Jo HS, Chang YH
- KMID: 1426767
- J Lab Med Qual Assur.
- 2012 Dec;34(2):113-117.
Alpha-thalassemia (alpha-thalassemia), which is prevalent in the Mediterranean region, is caused by deficient synthesis of the alpha-globin chains. It is commonly caused by HBA1 and/or HBA2 gene deletion and is... -
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