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Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb Sallanches
Prashant Warang1, Sona Nair, Anita Nadkarni
1National Institute of Immunohaematology, Indian Council of Medical Research, King Edward Memorial Hospital Campus, Mumbai, India.
Abstract:
We report a 6-year-old child with Hb H disease due to homozygosity for Hb Sallanches [alpha104(G11)Cys-->Tyr], an unstable alpha2 chain variant. This child presented with a hemolytic anemia of intermediate severity and had never been transfused. This variant often remains undetected in the heterozygous state.
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