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Thalassemia

Hematologic Disorder

Overview

Thalassemia is inherited hemoglobin disorder causing chronic anemia (alpha or beta).

Symptoms

  • Anemia
  • Growth failure
  • Splenomegaly
  • Bone deformities

Diagnosis

  • Hb electrophoresis
  • MCV <70
  • Genetic testing

Treatments

  • Transfusion
  • Iron chelation (deferasirox)
  • BMT (cure)

Risk Factors

⚠️Consanguinity
⚠️Mediterranean/Asian ancestry

Key Facts

  • ℹ️Carrier 1.5% world
  • ℹ️Beta major: transfusion-dependent

ICD-10: D56 | Prevalence: yaygın (endemik)

Last updated: 11/9/2025