Yerevan
EN
Lab tests
42-112

Genetic diagnosis of alpha-thalassemia (mutations in the HBA gene)

Description

Alpha-thalassemia is an autosomal recessive genetic disease characterized by reduced production of globin alpha chains and accumulation of excess beta and gamma chains with the deposition of precipitates in erythroid lineage cells and the subsequent development of hemolytic anemia.

Period of execution

Within 14 days. The specified time does not include the day of biomaterial collection

Biomaterial type

  • Venous blood
Total price
59465 ֏
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Lab tests
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