B​​eta thalassemia is an inherited blood disorder, which is caused by an abnormal gene. 

​A person with thalassemia is unable to produce normal, functioning hemoglobin in the blood. Hemoglobin carries oxygen from the lungs to all parts of the body. When the body is not able to produce normal, functioning hemoglobin, the affected person suffers from anemia. 

Thalassemia​ is passed on from parent to child and can affect both males and females. In Singapore, about 3% of the population are carriers of the thalassemia gene. 

What are the Types of Thalassemia? 

There are two types of thalassemia​: 

  • ​​Thalassemia minor (thalassemia trait) 
  • Thalassemia major 

A person who has inherited one thalassemia gene is said to have thalassemia minor (thalassemia trait). He or she is healthy and leads a normal life.​ Most people with thalassemia minor do not know they have it. However, the affected persons can pass on the abnormal gene to their children. 

Thalassemia major is a severe form of anemia. The affected person has inherited two thalassemia genes, one from each parent. He or she may look normal at birth but within 1–2 years of life, will suffer from severe anemia, which leads to poor growth and development as well as a shorter lifespan. 

The affected person will need a blood transfusion every month to sustain life. At present, a bone marrow transplant is the only hope of possible cure for thalassemia major.​ 


Alpha thalassemia is a separate condition, which may be tested in specific cases using special DNA test. 

Alpha thalassemia occurs when one or more of the four alpha blood chain genes fails to function. 

This condition can be that of a silent carrier (one or two genes deletion), blood-transfusion dependent (three genes deletion) or fatal (four genes deletion).

​How is Thalassemia Inherited? 

If only one parent has thalassemia minor, the following can occur: 

  • 50% chance of having a child with thalassemia minor 
  • 50% chance of having a normal child ​
  • None of the couple’s children will get thalassemia major. 

If both parents have thalassemia minor, the following can occur: 

  • 25% chance of having a child with thalassemia major 
  • 50% chance of having a child with thalassemia minor 
  • 25% chance of having a normal child. 

The chances are the same with each pregnancy, no matter how many children the couple may have.​ 

Who Should Go for Thalassemia Screening? 

Since thalassemia can be passed on from one generation to another, you and your partner should go for a thalassemia screening​ if you are: 

  • Planning to get married 
  • Starting a family. 

Thalassemia screening involves a simple blood test which is readily available. 

What Should I Do if I Have Thalassemia Minor? 

If you or your partner have thalassemia minor, both of you should see a doctor for genetic counseling before you plan to get married or have a child. 

The doctor will explain the risks and discuss the choices you have. He may refer you to the National Thalassemia Registry for further counseling. The National Thalassemia Registry provides genetic counseling for people with thalassemia and screening for their families. ​

What if I Am Already Pregnant? 

If you are already pregnant and both you and your husband have thalassemia, you should go for a prenatal diagnostic test to find out whether your unborn baby has thalassemia major. Prenatal diagnosis can be done by chorionic​ villus sampling or amniocentesis (read the article on Down Syndrome Tests). 

Based on the results of the test, the doctor will advise you accordingly.​ 


Source: Dr TAN Thiam Chye, Dr TAN Kim Teng, Dr TAN Heng Hao, Dr TEE Chee Seng John, The New Art and Science of Pregnancy and Childbirth, World Scientific 2008. 

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