Demographic and Clinicoradiological Presentation of Tuberculosis in Patients with Sickle Cell Haemoglobinopathy: A Cross-sectional Studydoi:10.7860/JCDR/2022/53298.16650INDIATUBERCULOSIS patientsSICKLE cell anemiaSICKLE cell traitCROSS-sectional methodIntroduction: Infectious disease is an ...
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Beta S-globin gene (#946;S-globin) haplotypes, markers for severe sickle cell anemia (SCA), and the alpha-thalassemia 2 gene 3.7 kb deletion (-#945;2(3.7 kb) thal) along with demographic and clinical data were investigated in SCA outpatients (n = 125, 63 female and 62 male) in the...
M. (2023). Psychosocial challenges of persons with sickle cell anemia: A narrative review. Medicine, 102(47), e36147. https://doi.org/10.1097/MD.0000000000036147 Article PubMed PubMed Central Google Scholar McPherson, M., Thaniel, L., & Minniti, C. P. (2009). Transition of patients ...
Time to invest in sickle cell anemia as a global health priority. Pediatrics. 2016;137(6). https://doi.org/10.1542/peds.2016-0348. National Population Commission (NPC) [Nigeria] and ICF. Nigeria Demographic and Health Survey 2018. 2019. https://dhsprogram.com/pubs/pdf/FR359/FR359.pdf....
Abbreviations SCH: Sickle cell hepatopathy SCD: Sickle cell disease HbS: Hemoglobin S SS: Sickle cell anemia SC: Sickle cell/hemoglobin C SB: Sickle/β thalassemia VOCs: Vaso-occlusive crisis MRCP: Magnetic resonance cholangiopancreatography ...
Sickle cell anemia (SCA) is associated with a chronic proinflammatory state characterized by elevated leukocyte count, mortality from severe recurrent infections, and subsequent vasoocclusive complications with leukocyte adhesion to the endothelium and increased plasma levels of inflammatory cytokines. The ...
Method: This is a descriptive and quantitative study, based on a population of 15 children with sickle cell disease. The demographic, socioeconomic and clinical characteristics were collected through the use of a form containing structured questions, applied to the mothers/tutors of the children. ...
Loggetto, S. R. Sickle cell anemia: clinical diversity and beta S-globin haplotypes.Rev. Bras. Hematol. Hemoter.35, 155–7 (2013). ArticleGoogle Scholar Steinberg, M. H. & Sebastiani, P. Genetic modifiers of sickle cell disease.Am. J. Hematol.87, 795–803 (2012). ...
Pneumococcal conjugate vaccine POCT: Point-of-care test SCA: Sickle cell anemia SCD: Sickle cell disease SPARCO: Sickle Pan-African Research Consortium SPIN: Stroke Prevention In children with sickle cell anaemia in Nigeria USA: United States of America WHO: World Health Organization ...