Google
Trusted Resources: News & Events
Latest announcements and gatherings
Study Suggests Ways of Improving Newborn Screening for Sickle Cell Disease
Researchers in Spain have defined cutoff points in hemoglobin measuring that can improve sensitivity and specificity to neonatal screening for sickle cell disease (SCD). Scientists can apply the method to diagnose other blood disorders, leading to better neonatal care.
Their report, “Impact of prematurity and immigration on neonatal screening for sickle cell disease,” appeared in the scientific journal PLOS One.
Measuring levels of different hemoglobins in infants is essential in diagnosing SCD. Previous research had described the relationship among hemoglobin A levels, the duration of the pregnancy, the baby’s gender and the mother’s ethnicity. However, those studies never defined normal cutoff points for different neonatal hemoglobins that took such factors into account, thereby compromising the sensitivity of these diagnostic tests.
+myBinderRelated Content
-
SCDAA Partners With Phi Beta Sigma FraternityThe Sickle Cell Disease Association of A...
-
Managing Chronic Illness in CollegeStarting college presents a unique set o...
-
Fighting Painful Misconceptions About Sickle Cell Disease in the ERWhen sickle cell patients arrive at emer...
-
MARAC Advisory Statement: Update About COVID-19December 23, 2021 – The Sickle Cell Di...
-
Sickle Cell Disease isn’t Laughable, But It Has a Comedic Ambassador — Kier “Junior” SpatesMr. Spates believes in living a full lif...
-
Reproductive Issues for Women With Sickle Cell Diseasehttps://www.youtube.com/watch?v=4vo_BPBn...
-
Sickle Cell Disease Association of America, Inc. Awards Community Based Organizations With $2,033,080 for Newborn Sc...The Sickle Cell Disease Association of A...
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.
Powered by
Support for this site is provided by
This platform is made possible through a partnership with the Sickle Cell Disease Association of America, Inc. (SCDAA) and its member organizations. SCDAA's mission is to advocate for people affected by sickle cell conditions and empower community-based organizations to maximize quality of life and raise public consciousness while advancing the search for a universal cure.