Also known as: hemoglobin E disease, HbE.
What is hemoglobin E?
Hemoglobin is the protein in the blood that carries oxygen from the lungs throughout the body. One abnormal form of hemoglobin is known as hemoglobin E. Hemoglobin E disease is a mild disorder, and people who have it may have no symptoms or mild anemia.
What causes hemoglobin E?
Hemoglobin E is a genetic disorder that is passed along from parents to their children. Both parents pass along the trait in order for the child to develop the disorder.
What are the symptoms of hemoglobin E?
In most cases, hemoglobin E does not cause any symptoms. However, it can cause mild anemia, which can lead to symptoms such as pale skin, tiredness and fatigue.
What are hemoglobin E care options?
There is no cure for hemoglobin E. Treatments typically involve preventing potential complications and treating them as they arise.
Reviewed by: Athena Pefkarou, MD
This page was last updated on: 10/29/2018 10:21:25 AM
From the Newsdesk
Doctors in South Florida are performing a life-saving procedure for children born with a rare genetic condition: thalassemia.
Dr. Jorge Galvez Silva is a pediatric hematologist/oncologist with the Cancer & Blood Disorders Center at Nicklaus Children's Hospital. For more information, please visit nicklauschildrens.org/cancer