Haematologica, Vol 90, Issue 4, 551-552
Copyright © 2005 by Ferrata Storti Foundation
A new polyadenylation site mutation associated with a mild beta-thalassemia phenotype
PC Giordano,
MJ Bouva,
P Van Delft,
N Akkerman,
MC Kappers-Klunne,
and
CL Harteveld
At least 180,000 autochthonous and allochthonous people are carriers of a large spectrum of hemoglobinopathies in The Netherlands. We describe two cases, the first, a 33-year old Surinamese Creole woman, studied because of an intermediate hemolytic anemia; the second, a couple requesting analysis because of a previously diagnosed carrier state in the male partner, while the carrier state in the pregnant female was uncertain.