4.4: Thalassemia
- Page ID
- 38796
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Images show thalassemia peripheral blood smears with hypochromic, microcytic red blood cells and poikilocytosis. From MLS Collection, University of Alberta.
Image 1: 50x oil immersion. https://doi.org/10.7939/R3DR2PQ4J
Image 2: 50x oil immersion. https://doi.org/10.7939/R3V698T05
Image 3: 50x oil immersion. https://doi.org/10.7939/R3HD7P773
Thalassemias are classified as a group of genetic hemoglobin disorders where the production of α and β globin chains is affected. This is considered to be a quantitative hemoglobin disorder and is categorized by the affected globin chain (alpha or beta), and as major or minor depending on the severity of the disease.1,2
Alpha-Thalassemia:
Cause(s):
α globin chain genes are located on chromosome 16 and there are normally four genes in total (αα/αα), two inherited from each parent. α-thalassemia results when there is a deletion in any number of the α globin gene. The severity of anemia and amount of α globin chain production is dependent the number of genes that are deleted.3
α-Thalassemia Silent Carrier (αα/α-):1,2
Occurs when one α gene is deleted. There is still adequate production of α to ensure normal hemoglobin synthesis. Patient is asymptomatic and the mutation is benign.
In newborns, there is an excess production of γ globin chains. These γ globin chains tend to also form tetramers and result in Hemoglobin Barts (Hb Barts). Hb Barts has a high oxygen affinity and is inefficient for oxygen delivery to the tissues of the developing fetus. In the silent carrier state, there is only a small amount of Hb Barts produced.
α-Thalassemia Minor (αα/–) or (α-/α-):1,2
Occurs when two α genes are deleted. There is now a 50% reduction in normal α globin chain production.
In adults, increased production of red blood cells is able to compensate for the decrease in α chain production, and α and β globin chain production is balanced. Patients are asymptomatic and any anemia present is mild.
There is between 5-15% hemoglobin Barts present at birth, but this decreases once β globin chain production takes over and γ globin chain production decreases. In adults, globin chain production is balances, so no Hemoglobin H is formed.
Hemoglobin H Disease (α-/–):1,2