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We observed a case of hereditary spherocytosis who was a 4-month-old boy with the
chief complaints of jaundice and pallor. Evidence of the same disease was also found in the
patient` s father who had never been symptomatic.
Diagnosis was made by presence of spherocytes in peripheral blood smear, osmotic fragility-
test and autohemolysis test.
A brief review of literatures was made.
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