MARTIN H. STEINBERG, M.D., F.A.C.P.; BERNARD J. DREILING, M.D., F.A.C.P.
STEINBERG MH, DREILING BJ. Glucose-6-Phosphate Dehydrogenase Deficiency in Sickle-Cell Anemia: A Study in Adults. Ann Intern Med. 1974;80:217-220. doi: 10.7326/0003-4819-80-2-217
Download citation file:
Published: Ann Intern Med. 1974;80(2):217-220.
There is evidence that the prevalence of G-6-PD deficiency is greater than would be expected in individuals with sickle-cell anemia, which suggests a survival advantage for these patients. We have studied 45 individuals with sickle-cell anemia, with methods for detecting G-6-PD deficiency in the presence of reticulocytosis, and we have found its prevalence to be similar to that of control subjects. The patients were mostly adults with mild sickle-cell disease. The differences between our findings and those reported previously may be partly owing to the nature of the populations studied. Our findings do not provide evidence that G-6-PD deficiency in adults with sickle-cell anemia gives them any advantage in survival.
Learn more about subscription options.
Register Now for a free account.
Hematology/Oncology, Red Cell Disorders.
Results provided by:
Copyright © 2017 American College of Physicians. All Rights Reserved.
Print ISSN: 0003-4819 | Online ISSN: 1539-3704
Conditions of Use
This PDF is available to Subscribers Only