Medical Definition of Hemoglobin S

Hemoglobin S: The most common type of abnormal hemoglobin and the basis of sickle cell trait and sickle cell anemia.

Hemoglobin S differs from normal adult hemoglobin (called hemoglobin A) only by a single amino acid substitution (a valine replacing a glutamine in the 6th position of the beta chain of globin). Recognition of this tiny change in the hemoglobin molecule marked the opening of molecular medicine.

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Reviewed on 12/12/2018