Sickle cell anemia, sickle cell β-thalas
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Enis Boletini; Martina Svobodova; Vladimir Divoky; Erol Baysal; Mehmet A. Cürük;
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Article
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1994
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Springer
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English
⚖ 569 KB
We have analyzed the hemoglobin abnormalities in nearly 50 Albanian patients with a significant hemoglobinopathy and included 37 relatives in this study. Sickle cell anemia (SS) is a common disorder; all 15 sickle cell anemia patients had the complications expected for this disease. The beta S haplo