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Inherited, non‐spherocytic haemolysis due to deficiency of glucose‐6‐phosphate dehydrogenase

✍ Scribed by Ronquist, G.; Theodorsson, E.

Book ID
120045087
Publisher
Informa plc
Year
2007
Tongue
English
Weight
253 KB
Volume
67
Category
Article
ISSN
0036-5513

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## Abstract A 28‐year‐old asymptomatic male of Iranian Jewish (Meshadi) heritage was found on routine exam to have an erythrocytosis (RBC = 6.22 × 10^12^/l, Hgb = 19.2 g/dl, Hct = 58.9%). Splenomegaly was absent on physical exam. There was no family history of erythrocytosis. His oxygen dissociatio