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Thalassemia

A Genetic Blood Disorder That Affects Hemoglobin Production

About Thalassemia

Thalassemia is an inherited blood disorder in which the body produces an abnormal or reduced amount of hemoglobin. Hemoglobin is the protein in red blood cells responsible for carrying oxygen throughout the body. Due to defective hemoglobin production, red blood cells are destroyed faster than normal, leading to anemia.

Thalassemia is a lifelong condition that requires proper medical care and monitoring.

Types of Thalassemia

  • Thalassemia Minor (Trait)
    Mild form, often without symptoms. Usually detected during routine blood tests.
  •  Thalassemia Major
    Severe form requiring regular blood transfusions and lifelong treatment.
  • Thalassemia Intermedia
    Moderate severity, may require occasional transfusions.

Common Symptoms

Our Treatment

Regular Blood Transfusions

Maintain healthy hemoglobin and oxygen levels

Iron Chelation Therapy

Removes excess iron from the body

Folic Acid Supplements

Supports healthy red blood cell production

Bone MarrowTransplant

Potential curative treatment for severe cases

Supportive Care & Monitoring

Prevents complications and improves quality

Why Choose Us

FAQS

Is thalassemia curable?

Severe thalassemia can potentially be cured with a bone marrow or stem cell transplant. Other treatments help manage symptoms effectively.

No, thalassemia is a genetic disorder and does not spread from person to person.

Carrier screening and genetic counseling can significantly reduce the risk of severe thalassemia in children.

With proper treatment and regular monitoring, many patients live healthy and productive lives.

Feeling Constantly Tired

Recognizing thalassemia early can protect your child’s future health.