Disorders & Diseases
Thalassaemia is an inherited blood disorder. It happens when a child receives faulty haemoglobin genes from one or both parents.
Step-by-step:
- Haemoglobin is the protein inside red blood cells that carries oxygen.
- Haemoglobin is made of protein chains called alpha chains and beta chains.
- The instructions for making these chains are stored in genes.
- If there is a mutation (change) in these genes, the body cannot make enough normal haemoglobin.
- As a result, red blood cells become weak, small, and are destroyed more quickly than normal.
- This leads to anaemia (low number of healthy red blood cells).
How is it inherited?
If both parents are carriers of thalassaemia trait:
- 25% chance the child will have normal genes.
- 50% chance the child will be a carrier (thalassaemia minor).
- 25% chance the child will have thalassaemia major (severe disease).
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