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A case report of concomitant paroxysmal nocturnal hemoglobinuria and heterozygous β-thalassemia

✍ Scribed by Xiao-Lin Yin; Tian-Hong Zhou; Lin Peng; Xin-Hua Zhang; Li Wang; Ya-Li Zhou; Yong-Sheng Chen; Yuan-Yuan He

Publisher
Springer
Year
2010
Tongue
English
Weight
70 KB
Volume
90
Category
Article
ISSN
0939-5555

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The clinical and hematological parameters of a patient described here, who inherited the genes of both hereditary elliptocytosis (HE) and p-thalassemia, seem to reflect a mutual enhancement of the two diseases. The coexistence of the two pathologies is probably also responsible for the observed chan