The page below is a sample from the LabCE course Hemoglobinopathies: Hemoglobin S Disorders. Access the complete course and earn ASCLS P.A.C.E.-approved continuing education credits by subscribing online.

Learn more about Hemoglobinopathies: Hemoglobin S Disorders (online CE course) »
How to Subscribe
MLS & MLT Comprehensive CE Package
Includes 94 CE courses, most popular
$95 Add to cart
Pick Your Courses
Up to 8 CE hours
$50 Add to cart
Individual course$20 Add to cart

The Sickling Process, continued

The sickling process progresses through stages of nucleation, growth, and alignment.

Nucleation involves the aggregation of a small number of hemoglobin tetramers into clusters or short linear polymers. This stage is also called the lag phase. These clusters may be reversed upon re-oxygenation.

With each repeated occurrence, the polymers continue to grow. In this polymerization stage, the internal cellular viscosity increases.

Eventually the fibers that are formed become irreversible crystalline structures, which align into bundles, thus creating the pointed elongated and typically crescent-shaped morphologies associated with sickle cells (drepanocytes) as seen in the peripheral blood field below.