Hemoglobin E - Wikipedia
Hemoglobin E (HbE) is an abnormal hemoglobin with a single point mutation in the β chain. At position 26 there is a change in the amino acid , from glutamic acid to lysine (E26K). Hemoglobin E is very common among people of Southeast Asian , Northeast Indian , Sri Lankan and Bangladeshi descent.
Hemoglobin E Syndromes - American Society of Hematology
Jan 1, 2007 · Hemoglobin (Hb) E is one of the world’s most common and important mutations. It results in a heterogeneous group of disorders whose phenotype range from asymptomatic to severe. Hb E trait and Hb EE are mild disorders.
Hemoglobin E disease | About the Disease | GARD - Genetic and …
Hemoglobin E (HbE) disease is a mild, inherited blood disorder characterized by an abnormal form of hemoglobin, called hemoglobin E. People with this condition may have very mild anemia, but the condition typically does not cause any symptoms.
Hemoglobin E trait is a condition that affects the red blood cells. Your red blood cells contain hemoglobin, which carries oxygen from the lungs to all parts of your body.
The Hemoglobin E Thalassemias - PMC - National Center for …
Hemoglobin E (HbE) is an extremely common structural hemoglobin variant that occurs at high frequencies throughout many Asian countries. It is a β-hemoglobin variant, which is produced at a slightly reduced rate and hence has the phenotype of a mild form of β thalassemia.
Hemoglobin E Trait - Stanford Medicine Children's Health
Hemoglobin E trait is an inherited blood disorder. That means it is passed down through your parent’s genes. It leads to an abnormal form of hemoglobin that may cause mild anemia. It occurs most often in people of Southeast Asian descent.
Hemoglobin E Disease - Hemoglobin E Disease - The Merck …
Homozygous hemoglobin E (Hb E) disease is a hemoglobinopathy that causes a mild hemolytic anemia, usually without splenomegaly. (See also Overview of Hemolytic Anemia.) Hemoglobin (Hb) E is the third most prevalent hemoglobin worldwide (after Hb A and Hb S).
Hemoglobin variants including Hb C, Hb D, and Hb E - UpToDate
May 13, 2024 · This topic discusses genetic variants in globin genes. This includes especially common variants that produce hemoglobin (Hb) C, D, E, and others. An approach to Hb C genetic test results is presented separately. (See "Gene test interpretation: Hemoglobin C (Hb C) variant in the hemoglobin beta locus (HBB)".) Separate topic reviews discuss the ...
Hemoglobin E Trait - Nationwide Children's Hospital
Mar 1, 2022 · Hemoglobin E trait is an inherited blood disorder. That means it's passed down through your parent’s genes. It leads to an abnormal form of hemoglobin that may cause mild anemia. It occurs most often in people of Southeast Asian descent.
Hemoglobin E - an overview | ScienceDirect Topics
Hb E is a structurally abnormal hemoglobin that results from an amino acid substitution (lysine for glutamine) at the number 26 amino acid of beta globin, counting from the N terminus. Because this mutation also adversely affects mRNA processing, there is …