A Rare Case of Co-Inheritance of Beta Thalassemia Intermedia and Coagulation FVII Deficiency

نویسندگان
Barati Shourijeh, Zahra ID 1
Karimi, Mehran ID 2

1 Department of Biochemistry, Islamic Azad University, Fars Science and Research Branch, Shiraz, Iran

2 Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

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چکیده

We present a 34-year-old man with combination of beta thalassemia intermedia and coagulation factor VII deficiency who was presented with pallor and irregular nose bleeding episodes. On physical examination, he had splenomegaly and yellow sclera. Pallor and splenomegaly could be reminder of thalassemic syndromes or hemoglobinopathies including thalassemia intermedia. Association with ...

کلیدواژه‌ها
Thalassemia intermedia, Factor VII deficiency, Coinheritance, Liver failure, Hypercoagulability, Bleeding tendency