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thalassemia minor

pathology
Also known as: heterozygous beta-thalassemia

Quick Summary

Thalassemia minor is a mild form of thalassemia, a group of blood disorders characterized by a deficiency of hemoglobin, the protein that transports oxygen. It is associated with a heterozygous condition for the gene involved, meaning an individual inherits one affected gene and one normal gene.12

People with thalassemia minor typically experience slight or no anemia and have a normal life expectancy. The condition is more common in individuals with ancestry from the Mediterranean, the Middle East, and southern Asia. It is believed that carrying the thalassemia gene may offer some protection against malaria in those who are heterozygous for it.2

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