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An 8-year-old male presented with severe pain in lower limbs, weakness, and jaundice, with a history of sickle cell trait in the family. Examination revealed anemia, hepatomegaly, and splenomegaly, with lab results indicating significant levels of HbS. The case is suggestive of Sickle Cell Anemia (SS) with Vaso-occlusive Crisis.

Author

Manjiri Kuthe

Language

EN