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Browsing by Author "Kundu, Chanchal"

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    Mild to Severe Anemia of Undiagnosed Etiology Diagnosed by Genetic Study
    (Nepal Paediatric Society (JNPS), 2016) Bose, Kalliol; Siddique, Md Abu Bakkar; Ghorai, Sudipta; Kundu, Chanchal; Saha, Sudip
    Abstract: We report a case of a child with beta thalassemia major, whose mother is a carrier of beta thalassemia and father is having hereditary persistence of fetal hemoglobin. Gene study revealed compound heterozygous for codon 8/9+G and IVS-1-5 G>C point mutation. Another four cases of anemia not responding to iron diagnosed to have alpha thalassemia carrier are also reported here.

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