Birth Prevalence of Sickle Cell Disease and County-Level Social Vulnerability — Sickle Cell Data Collection Program, 11 States, 2016–2020

Author:

Kayle Mariam,Blewer Audrey L.,Pan Wei,Rothman Jennifer A.,Polick Carri S.,Rivenbark Joshua,Fisher Elliott,Reyes Camila,Strouse John J.,Weeks Shelby,Desai Jay R.,Snyder Angela B.,Zhou Mei,Sutaria Ankit,Valle Jhaqueline,Horiuchi Sophia S.,Sontag Marci K.,Miller Joshua I.,Singh Ashima,Dasgupta Mahua,Janson Isaac A.,Galadanci Najibah,Reeves Sarah L.,Latta Krista,Hurden Isabel,Cromartie Shamaree J.,Plaxco Allison P.,Mukhopadhyay Ayesha,Smeltzer Matthew P.,Hulihan Mary

Publisher

Centers for Disease Control MMWR Office

Reference9 articles.

1. Trends in sickle cell disease-related mortality in the United States, 1979 to 2017.;Payne;Ann Emerg Med,2020

2. Evolutionary history of sickle-cell mutation: implications for global genetic medicine.;Esoh;Hum Mol Genet,2021

3. Perspectives of individuals with sickle cell disease on barriers to care.;Phillips;PLoS One,2022

4. Emergency department management of acute pain episodes in sickle cell disease.;Tanabe;Acad Emerg Med,2007

5. CDC. Sickle cell disease: about CDC’s work on sickle cell disease. Atlanta, GA: US Department of Health and Human Services, CDC; 2023. Accessed July 17, 2023. https://www.cdc.gov/ncbddd/sicklecell/about.html#:~:text=CDC%20strives%20to%20educate%20people,SCD%20among%20the%20general%20public

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