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Pseudomoyamoya in sickle cell anemia
Surgical Neurology, 1982Sickle cell (drepanocytic) anemia is a hereditary blood disease occurring very rarely in Mexico. A 13-year-old Mexican boy with sickle cell anemia eventually died of a cerebrovascular accident of the brain stem, as shown by computerized tomography (CT).
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TREATMENT OF SICKLE CELL ANEMIA
Archives of Internal Medicine, 1954SICKLE cell anemia was described first by Herrick in 1910. 1 Since then, surveys of Negroes in the United States have revealed the incidence of the symptomless sickle cell trait to be about 9% and incidence of sickle cell anemia to be about 2.25 per thousand.
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Thrombocytosis in Sickle Cell Anemia
Archives of Pediatrics & Adolescent Medicine, 1997In the July 1996 issue of theArchives, Quintana et al1described an adolescent girl with sickle cell anemia and extreme thrombocytosis (platelet count, 2×1012/L). We2,3have also described thrombocytosis in patients with sickle cell anemia; their platelet counts were higher than those in children who underwent splenectomy, but did not exceed 106/L.
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Metabolic bone diseases in sickle cell anemia patients and evaluation of associated factors
American Journal of the Medical Sciences, 2022Gul Ilhan
exaly