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Treatment with hydroxyurea in a patient compound heterozygote for a high oxygen affinity hemoglobin and β-thalassemia minor

✍ Scribed by Pierre-Olivier Gaudreau; Xiaoduan Weng; Ghislain Cournoyer; Louise Robin; Carmen Gagnon; Denis Soulières


Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
642 KB
Volume
84
Category
Article
ISSN
0361-8609

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## Abstract A 21‐year‐old man with homozygous sickle cell disease maintained on hydroxyurea for 1 year developed thrombosis of the superior sagittal, right transverse, and right sigmoid dural sinuses with a large venous infarct. He was successfully treated with endovascular thrombolysis. Investigat