Hgb E Disease
Also known as: hemoglobin E disease, HbE.
What is Hgb E disease?
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. Hgb E disease is a mild disorder, and people who have it may have no symptoms or mild anemia.
What causes Hgb E disease?
Hgb E disease is a genetic disorder that is passed along from parents to their children. Both parents must pass along the trait in order for the child to develop the disorder.
What are the symptoms of Hgb E disease?
In most cases, Hgb E disease 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 Hgb E disease care options?
Treatments typically involve preventing potential complications and treating them as they arise.
Reviewed by: Athena Pefkarou, MD
This page was last updated on: September 30, 2020 12:00 PM