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 97 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

Clinical Manifestations of Sickle Cell Disease (SCD)

SCD manifests as a chronic hemolytic anemia. In addition to the general symptoms of anemia (fatigue, weakness, pallor etc.) patients are prone to infection, cardiomegaly (usually due to iron deposits from frequent transfusions), and bone and organ infarcts. Male patients can experience priapism. Children with SCD experience slowed growth and development.

Patients with SCD can experience vaso-occlusive crisis, hemolytic crisis, sequestration crisis, and aplastic crisis. The main symptom in SCD is pain. Pain is a warning sign that is related to vaso-occlusion and life-threatening complications.