HBEL — Thalassaemia Screen

Description

A COMPLETE SET OF TESTS THAT CHECK: • Genetic mutations or deletions in α-globin or β-globin genes that cause thalassemia traits • Whether an individual is a carrier (heterozygous) or potentially has a more severe form • Carrier status even if there are minimal or no symptoms WHAT THIS TEST SUITE REVEALS: • If the person carries a thalassemia gene variant that could be passed to children • The specific type of mutation or deletion (alpha or beta) present • Whether additional testing or genetic counseling is indicated • Important information for family planning, especially in populations at risk • Helps differentiate unexplained anemia from iron deficiency or thalassemia trait

Biomaterial

Venous blood

Preparation

No special preparation required