Silent brain infarcts in adult Kuwaiti sickle cell disease patients
β Scribed by R. Marouf; R. Gupta; M.Z. Haider; A.D. Adekile
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 75 KB
- Volume
- 73
- Category
- Article
- ISSN
- 0361-8609
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## Abstract Sickle cell disease (SCD) is associated with early mortality. We sought to determine the incidence, cause, and risk factors for death in an adult population of patients with SCD. All patients aged β₯18 years seen at the Adult Sickle Cell Center at Duke University Medical Center between J
The clinical and biological heterogeneity of sickle cell hemoglobin (Hb) C disease (SC disease) is similar to sickle cell anemia, but has a much milder course. The effect of genetic factors such as β£ thalassemia or β€-globin gene haplotype has been analyzed in a limited number of cases. In this work,