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- W2124162105 abstract "Compound heterozygosity for bS/bD results in a severe hemolytic anemia and a clinical syndrome similar to that of sickle cell disease. Here, we report a case of HbSD Punjab disease. A 10 year old female child residing at Nagpur, Maharashtra presented with severe hemolytic anemia, hepatosplenomegaly and occasional pains in bones and abdomen. Initially, she was thought to be a case of sickle cell anemia, however, with the help of HPLC and molecular analysis it was confirmed as HbSD Punjab disease." @default.
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- W2124162105 date "2005-01-01" @default.
- W2124162105 modified "2023-09-27" @default.
- W2124162105 title "Hemoglobin sickle D Punjab-a case report" @default.
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- W2124162105 doi "https://doi.org/10.4103/0971-6866.19536" @default.
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