Shrestha, BikashKarmacharya, KavitaSingh, JasjitKotwal, JyotiDevgan, Amit2026-06-022026-06-022011https://hdl.handle.net/20.500.14572/6331Bikash Shrestha Resident, Department of Pediatrics, Armed Forces Medical College, Pune Kavita Karmacharya Department of Pathology, Armed Forces Medical, College, Pune Jasjit Singh Department of Medicine, Clinical Hematology and Oncology, Command Hospital, Southern Command, Pune Jyoti Kotwal Associate Professor and Senior Advisor, Department of Pathology, Armed Forces Medical, College, Pune Amit Devgan Associate Professor, Department of Pediatrics, Armed Forces Medical College, Pune, IndiaAbstract: 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.en-USSickle cell diseasehemoglobinopathythalassemiahydroxyureaglobinelectrophoresisHPLCArticle