Abstract
Sickle cell disease is a type of hemoglobinopathy, which is fairly common in certain parts of the world. We would like to report an interesting case of a child who was labeled as sickle cell anemia but subsequently turned out to be a case of compound heterozygous sickle cell and thalassemia trait.
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Shrestha, B., Karmacharya, K., Singh, J., Kotwal, J., & Devgan, A. (2011). Compound heterozygous sickle and thalassemia trait: A case report. Journal of Nepal Paediatric Society, 31(2), 130–133. https://doi.org/10.3126/jnps.v31i2.4414
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