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We experienced a case of hereditary spherocytosis patient who was in a recovery phase of aplastic
crisis at the time of presentation. This was a 7 years old boy with complaints of pallor and intermit-
tent abdominal pain. Asymptomatic jaundice was also found in the patient's grandfather and two
maternal uncles. Patient’s mother had splenectomy due to hereditary spherocytosis.
Diagnosis was made by morphology,... |
