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Postgraduate Medicine Volume 43, 1968 - Issue 3
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Original Articles

Hemoglobins and Heredity

Second of Two Parts

Kenneth L. Becker
, M.D. (EDITOR) &
Paul HellerUniversity of Illinois College of Medicine, Chicago
, M.D.
Pages 91-94 | Published online: 18 Apr 2016
 
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Abstract

Patients with sickle cell anemia now survive into adulthood, and adults with the disease have problems—infarcts of various organs, cardiomegaly, postnecrotic cirrhosis and eye changes. Sickle cell trait rarely causes problems, but Hb CS and Hb C disease give rise to mild anemias.

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