Sickle cell disease refers to a group of disorders resulting from mutations in the hemoglobin gene that can lead to deformation of the red blood cell (RBC) into a crescent, or sickle, shape. From: Pediatric Emergency Medicine, 2008 About this pageAdd to MendeleySet alert ...
Apnea After 2-Month Vaccinations in Hospitalized Preterm Infants Original Investigation January 6, 2025 This Issue Other Articles August1923 SICKLE CELL ANEMIAREPORT OF TWO CASES IN CHILDREN, WITH NECROPSY IN ONE CASE V. P. SYDENSTRICKED, M.D.;W. A. MULHERIN, M.D.;R. W. HOUSEAL, M.D...
The Sickle Cell Treatment Market size is estimated at USD 3.32 billion in 2024, and is expected to reach USD 6.11 billion by 2029, growing at a CAGR of 12.98% during the forecast period (2024-2029). The impact of the COVID-19 pandemic on the studied market was significant. For instance...
The main sources of information are the Jamaican Cohort Study of Sickle Cell Disease, which was initiated in 1973 and followed up all individuals with SCD detected among 100,000 consecutive deliveries in Kingston, Jamaica6, and, in the United States, the Cooperative Study of Sickle Cell ...
Newborn screening—All states require that newborns be screened for sickle cell anemia, as well as some other hemoglobin disorders. Carrier screening—It is recommended that all pregnant women or those considering pregnancy receive information regarding carrier screening for hemoglobin disorders, including...
Sickle Cell Disease Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity and Forecast 2024-2034 Report Format:PDF+Excel |Report ID:SR112024A6460 Market Overview: The 7 major Sickle Cell Disease markets reached a value of US$ 775.7 Million in 2023. Looking forward, IMARC Group...
Book Reviews : Sickle Cell Disease: Basic Principles in Clinical Prac tice. S. H. Embury, R. P. Hebbel, N. Mohandas, and M. H. Steinberg (eds.). Raven Press, New York, NY, 1994, 902 pp., $145doi:10.1177/107602969500100115Rodger...
Additional Information How to Cite (2010), Sickle cell disease. J. Hosp. Med., 5: 35–36. doi: 10.1002/jhm.737 Publication History Issue published online: 8 APR 2010 Article first published online: 8 APR 2010 SEARCH Search Scope Search String Advanced > Saved Searches > SEARCH BY ...
Anne Yardumian5 and Kathleen Mulligan1,2* Abstract Background: The Adult Sickle Cell Quality of Life Measurement Information System (ASCQ-Me) has been shown to be a reliable and valid questionnaire measuring health-related quality of life (HRQoL) in the US sickle cell disease (SCD) population...
There is rather little information on the natural history of SCD (which is relevant for SCD prevention and control), especially in areas of high prevalence. The main sources of information are the Jamaican Cohort Study of Sickle Cell Disease, which was initiated in 1973 and followed up all ind...