Welcome to CDC stacks | Age trends in the prevalence of the sickle cell trait. - 62648 | Public Health Reports
Stacks Logo
Advanced Search
Select up to three search categories and corresponding keywords using the fields to the right. Refer to the Help section for more detailed instructions.
 
 
Help
Clear All Simple Search
Advanced Search
Age trends in the prevalence of the sickle cell trait.
  • Published Date:
    Nov 1973
  • Source:
    Health Serv Rep. 88(9):804-807
  • Language:
    English
Filetype[PDF-640.96 KB]


Details:
  • Supporting Files:
    No Additional Files
You May Also Like:
  1. Longitudinal data collection for sickle cell disease in California : history, goals and challenges
    Personal Author:
    Paulukonis, Susan T.; Raider, Faith; Hulihan, Mary M.;
    Corporate Author:
    Public Health Institute (Calif.). California Rare Disease Surveillance Program.. Public Health Institute (Calif.). California Environmental Health Trackin Program.. National Center on Birth Defects and Developmental Disabilities (Centers for Disease Control and Prevention). Division of Blood Disorders.. Pfizer, Inc.. Biogen, Inc.. CDC Foundation..
    Published:
    December 2015
    Description:
    Sickle cell disease (SCD) is the most common severe genetid disease. It impacts approximately 7,000 people in California and nearly 90,000 in the U.S. And yet remarkably little is known about the population impacted by SCD as a whole. Only recently h...
    File Type:
    Filetype[PDF - 922.47 KB]
  2. Registry and Surveillance System for Hemoglobinopathies -- RuSH : strategies from the field : Data collection
    Corporate Author:
    National Center on Birth Defects and Developmental Disabilities (Centers for Disease Control and Prevention). Division of Blood Disorders.. National Heart, Lung, and Blood Institute..
    Published:
    9/4/12
    Description:
    In 2010, the Registry and Surveillance System for Hemoglobinopathies (RuSH) pilot project was implemented by the Centers for Disease Control and Prevention (CDC) to collect state-specific, population-based data on people with sickle cell disease (SCD...
    File Type:
    Filetype[PDF - 4.05 MB]
  3. Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults
    Personal Author:
    Bean, Christopher J.; Hooper, W. Craig; Ellingsen, Dorothy; DeBaun, Michael R.; Sonderman, Jennifer; Blot, William J.;
    Published:
    Mar 28 2014
    Source:
    Public Health Genomics. 17(3):169-172.
    Description:
    Background : Sickle cell disease (SCD) is an autosomal recessive genetic disorder, with persons heterozygous for the mutation said to have the sickle cell trait (SCT). Serious adverse effects are mainly limited to those with SCD, but the distinction ...
    File Type:
    Filetype[PDF - 117.23 KB]
  4. Determinants of Anemia among Preschool Children in Rural, Western Kenya
    Personal Author:
    Foote, Eric M.; Sullivan, Kevin M.; Ruth, Laird J.; Oremo, Jared; Sadumah, Ibrahim; Williams, Thomas N.; Suchdev, Parminder S.;
    Published:
    Feb 04 2013
    Source:
    Am J Trop Med Hyg. 2013; 88(4):757-764.
    Description:
    Although anemia in preschool children is most often attributed to iron deficiency, other nutritional, infectious, and genetic contributors are rarely concurrently measured. In a population-based, cross-sectional survey of 858 children 6-35 months of ...
    File Type:
    Filetype[PDF - 599.20 KB]
  5. The Hypoxic Response Contributes to Altered Gene Expression and Pre-Capillary Pulmonary Hypertension in Patients with Sickle Cell Disease
    Personal Author:
    Zhang, Xu; Zhang, Wei; Ma, Shwu-Fan; Desai, Ankit A.; Saraf, Santosh; Miasniakova, Galina; Sergueeva, Adelina; Ammosova, Tatiana; Xu, Min; Nekhai, Sergei; Abbasi, Taimur; Casanova, Nancy G.; Steinberg, Martin H.; Baldwin, Clinton T.; Sebastiani, Paola; Prchal, Josef T.; Kittles, Rick; Garcia, Joe G. N.; Machado, Roberto F.; Gordeuk, Victor R.;
    Published:
    Feb 10 2014
    Source:
    Circulation. 129(16):1650-1658.
    Description:
    Background : We postulated that the hypoxic response in sickle cell disease (SCD) contributes to altered gene expression and pulmonary hypertension, a complication associated with early mortality. : Methods and Results : To identify genes regulated b...
    File Type:
    Filetype[PDF - 967.56 KB]