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3 Pages On Sickle Cells

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... basis of ethnicity include Tay-Sachs and Canavan diseases, thalassemias, and sickle cell anemia. The most common Women at risk for transmitting genetic disorders (eg, sickle cell disease, Tay-Sachs disease, cystic fibrosis) should be genetic vulnerabilities to certain illnesses (such as, for instance, sickle cell anemia) as well as possible treatments asked about drug use and whether they have sickle-cell anemia (Barker, 2001). Women at risk for transmitting genetic disorders (eg, sickle cell disease, Tay-Sachs disease, cystic fibrosis) should be ...



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Sources list for 3 PAGES ON SICKLE CELLS:

Charache, et. al. 1995. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell Anemia. N Engl J Med 332:1317-22.
Sickle Cell Disease

Platt, OS; Brambilla, DJ; Rosse, WF; Milner, PF; Castro, O; Steinberg, MH; Klug, PP. 1994. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N. Engl. J. Med 330: 1639-44.
Sickle Cell Disease

Powars, D, et al. 1993. Sickle cell anemia. Beta s gene cluster haplotypes as genetic markers for severe disease expression. Am. J. Dis. Child. 147:1197-1202.
Sickle Cell Disease

Powars, D, et. al. 1994. Beta-S gene cluster haplotypes modulate hematologic and hemorheologic expression in sickle cell anemia. Use in predicting clinical severity. Am. J. Ped. Hematology-Oncology 16:55-61.
Sickle Cell Disease

Kehinde MO, Akinsola FB. Ocular findings in sickle cell disease patients in lagos. Niger Postgrad Med J 2004;11:203-6.
Sickle Cell Retinopathy

 

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