October 1937


Author Affiliations


From the Department of Pediatrics and the Department of Pathology of Provident Hospital.

Arch Intern Med (Chic). 1937;60(4):623-653. doi:10.1001/archinte.1937.00180040059005

With the exception of the work reported by Diggs1 and that of Beck and Hertz,2 practically none of the articles on sickle cell anemia published in the past five years includes investigative work on the subject. It seems that knowledge of the disease has reached an impasse at present and that all writing henceforth must consist of case reports and summarizations of the literature until a new stimulus arises to give further impetus to the study of the condition and an understanding of the facts at hand. The present information on this disease has done no more than give possible leads to the cause of the sickling phenomena. No one has yet found the cause, and, most important from the standpoint of the patient, no one has found an effective therapeutic regimen or agent that will materially help the patient in the active anemic stage of the disease.

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