## Abstract In an ethnic group in southern India, the Irula, seven individuals with sickle cell anemia were found to manifest only mild illness. Although a relatively high level of fetal hemoglobin was present in one, none of the factors thought to ameliorate the course of sickling disorders could
Age and prevalence of sickle-cell trait in a large ambulatory population
โ Scribed by Dr. Oswaldo Castro; Sohail R. Rana; Ki Moon Bang; Roland B. Scott; D. C. Rao
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 307 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0741-0395
No coin nor oath required. For personal study only.
โฆ Synopsis
We performed hemoglobin electrophoresis in 30,400 apparently healthy black individuals in the Washington D.C. Metropolitan area, who were participating in a community based sickle-cell screening program during the period 1978-1985. The overall prevalence of sickle-cell trait was 6.7%. The frequency of sickle-cell trait in various age groups, which included young children, adults, and individuals over 65 years of age, ranged from 6.4 to 7.4%. There were no statistically significant differences in the prevalence of sickle-cell trait among the various age groups, nor did we detect a significant trend for increasing or decreasing sickle cell frequency with advancing age (P = 0.418). Thus, in this population sicklecell trait appears to have no effect on longevity. If the various complications of sickle-cell trait reported in the literature are not fortuitous, their frequency and/or severity must be too low to affect prevalence figures.
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## Abstract ## Background: Monoclonal Bโcells can be detected in the peripheral blood of some adults without Bโcell malignancies, a condition recently termed monoclonal Bโcell lymphocytosis (MBL). The risk of individuals with MBL progressing to a Bโcell malignancy is unknown. Polyclonal Bโcell lym