ERNEST W. SMITH; C. LOCKARD CONLEY, F.A.C.P.
Soon after the discovery that sickle (S) hemoglobin can be differentiated from normal (A) hemoglobin by electrophoresis,1 other abnormalities of hemoglobin were recognized. In studying a white patient who previously had been thought to have sickle cell anemia, Itano2 found that the erythrocytes of the mother could not be made to sickle, although the electrophoretic pattern was indistinguishable from that of sickle cell trait. The abnormal hemoglobin which did not produce sickling also differed from S hemoglobin because of its normal solubility in the reduced state, and was subsequently designated as hemoglobin D. The atypical hemolytic disorder in the patient
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SMITH EW, CONLEY CL. SICKLE CELL-HEMOGLOBIN D DISEASE(SICKLE CELL-HEMOGLOBIN D DISEASE*). Ann Intern Med. 1959;50:94–105. doi: 10.7326/0003-4819-50-1-94
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Published: Ann Intern Med. 1959;50(1):94-105.
Hematology/Oncology, Red Cell Disorders.
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Print ISSN: 0003-4819 | Online ISSN: 1539-3704
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