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W Moo-Penn, K Bechtel, D Jue, MS Chan, G Hopkins, NJ Schneider, J Wright and RM Schmidt
The first reported case of hemoglobin S and C Harlem in an individual is
described. The patient, a 35-yr-old female, had numerous crises during
adolescence and early adulthood, but these occurred more infrequently as
she grew older. Chemical evidence is presented for the characterization of
both variant hemoglobins. The clinical course of this individual with Hb S
in combination with Hb C Harlem appears to be similar to that for persons
with sickle cell anemia.
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| Copyright © 1975 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||