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Diseases & conditions
Blood

Thalassaemia

Thalassaemia is an inherited blood disorder in which the body makes too little or abnormal haemoglobin, causing anaemia. People with one changed gene (thalassaemia minor, or carriers) are usually healthy with mild anaemia. A child who receives the gene from both parents can have thalassaemia major, a serious illness that needs regular blood transfusions for life. It is common in Afghanistan and the region, and testing before marriage can prevent it.

Symptoms

  • Carriers (minor): usually no symptoms, or mild tiredness and pale skin
  • Major: severe paleness and weakness starting in the first 1 to 2 years of life
  • Major: poor feeding, slow growth and frequent infections
  • Major: yellow eyes, dark urine and a swollen belly from a large spleen or liver
  • Major: changes in the face and skull bones if not treated

When to see a doctor

Get medical help quickly if you notice any of these:

  • A baby or young child who is very pale, weak or not growing
  • Fever in a child with thalassaemia major, especially after spleen removal: seek care urgently
  • Shortness of breath, swelling of legs or palpitations in a person with thalassaemia
  • You are planning marriage or pregnancy and there is thalassaemia in the family
  • You have been told you are anaemic but iron does not help

In an emergency, go to the nearest hospital or clinic straight away.

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Causes

  • Inherited changes in the genes that make haemoglobin
  • If both parents are carriers, each child has a 1 in 4 chance of thalassaemia major
  • Marriage between relatives, such as cousins, increases the chance that both parents carry the same gene
  • It is not caused by infection, diet or anything the mother did in pregnancy

Prevention

  • Blood test (CBC and haemoglobin test) before marriage, especially between relatives
  • Genetic counselling for couples who are both carriers
  • Testing in early pregnancy where available for carrier couples
  • Family members of a person with thalassaemia should be tested

Treatment

  • Carriers usually need no treatment
  • Carriers should not take iron tablets unless a blood test shows iron deficiency
  • Thalassaemia major: regular blood transfusions, usually every 2 to 5 weeks, at a specialist centre
  • Medicine to remove extra iron from the body (iron chelation), prescribed by a specialist
  • Folic acid, vaccines and treatment of infections
  • Bone marrow transplant can cure some children in specialist centres

Common questions

Can two thalassaemia carriers marry?

They can, but each pregnancy has a 1 in 4 chance of a child with thalassaemia major. Couples should get genetic counselling before marriage or pregnancy to understand their options.

I have thalassaemia minor. Should I take iron for my anaemia?

Only if a blood test shows you are also low in iron. Taking iron when it is not needed can cause harmful iron build-up.

General information onlyThis guide does not replace an examination by a doctor. Do not start or stop a medicine without a doctor's advice.