What parents may notice
- Persistent anaemia
- Pallor and tiredness
- Poor growth
- Jaundice
- Enlarged spleen
- Need for repeated transfusions
- Family history or carrier parents
- Abnormal newborn or haemoglobin test
Thalassaemia is an inherited condition affecting haemoglobin production. Some children are healthy carriers, while others develop significant anaemia and may need regular transfusions and long-term monitoring. The exact type is determined through blood testing and, when appropriate, genetic evaluation.

Thalassaemia is inherited through gene variants passed by parents. It is not caused by diet or infection. Carrier couples benefit from genetic counselling about future pregnancies.
Not what we wish you'd ask. What you're actually thinking when you find this page.
Book a consultationNo. Carriers are usually well, while transfusion-dependent forms cause significant anaemia.
Only when iron deficiency is confirmed. Trait itself does not improve with routine iron.
Repeated transfusions can cause excess iron to collect in organs, so monitoring and chelation may be needed.
Stem-cell transplantation can be curative for selected children, while suitability depends on many clinical factors.
Parental carrier testing and genetic counselling can clarify inheritance and future-pregnancy risk.
Speak with Paediatric Haematology or contact our team to organise the right starting point.