Thalassemia

Thalassemia is a hereditary blood disorder caused by mutations in the genes responsible for producing hemoglobin chains—specifically the alpha and beta chains.

schedule2-6 weeks
paymentsFrom $5,000

Overview

Thalassemia is a hereditary blood disorder caused by mutations in the genes responsible for producing hemoglobin chains—specifically the alpha and beta chains. Hemoglobin is the protein in red blood cells that carries oxygen. The severity depends on how many gene mutations are inherited. It is most common in individuals from Asia, the Middle East, Africa, and Mediterranean countries like Greece and Turkey

Procedure Details

Inherited from parents through mutated hemoglobin genes. If both parents are carriers, the child has a high chance of developing a severe form. Symptoms usually appear in the first two years of life for moderate/severe cases. Transplanted cells begin producing healthy red blood cells within a month

verified Why Choose India

India's JCI and NABH-accredited hospitals offer international-standard outcomes at a fraction of US and UK prices, with shorter waiting times, English-speaking care teams, and dedicated international patient departments.

Cost Comparison

CountryEstimated Cost
United States$150,000
United Kingdom$70,000
India via Medvalley$5,000 – $25,000

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