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Condition Guide

Thalassemia

Inherited blood disorder requiring lifelong care

Medically reviewed by: Dr. Ajay Kumar Jha
Last updated: 2026-08-13
Sources: Nepal Medical Association, WHO, American Society of Hematology

What is Thalassemia?

Thalassemia is an inherited blood disorder where the body makes less hemoglobin than normal. It requires lifelong management and family counseling.

Symptoms

  • Pale or yellow skin
  • Facial bone deformities
  • Slow growth in children
  • Dark urine
  • Abdominal swelling
  • Fatigue

When to See a Doctor

Children with family history of thalassemia should be screened. Prenatal counseling is available for carrier couples.

Diagnosis

CBC, peripheral smear, hemoglobin electrophoresis, and genetic testing. Prenatal diagnosis available for at-risk pregnancies.

Management

Regular blood transfusions, iron chelation therapy, folic acid supplementation, and infection prevention. Bone marrow transplant is curative in selected cases.

Dr. Ajay Kumar Jha's Expertise

Dr. Jha runs one of Nepal's most experienced thalassemia care programs, offering comprehensive transfusion and chelation management.

Frequently Asked Questions

Thalassemia is an inherited blood disorder where the body makes less hemoglobin than normal. It requires lifelong management.
Bone marrow transplant can be curative in selected cases. Otherwise, regular transfusions and chelation therapy are the mainstay of treatment.
Carrier screening and genetic counseling can help prevent thalassemia. Prenatal diagnosis is available for at-risk couples.

Need a consultation?

Dr. Ajay Kumar Jha is available for appointments. Get expert care for your child or blood disorder.

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