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Oral and maxillofacial sequelae of sickle cell crises in a rare sickle cell disease genotype – HBS/β+-thalassemia

✍ Scribed by M.F. Kiernan; H. Ho; L. Cheng; T. Sato; Q. Naqvi; Z. Imran; R. Amos

Book ID
116563086
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
103 KB
Volume
40
Category
Article
ISSN
0901-5027

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✍ Enis Boletini; Martina Svobodova; Vladimir Divoky; Erol Baysal; Mehmet A. Cürük; 📂 Article 📅 1994 🏛 Springer 🌐 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