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Pune activists propagate compulsory thalassaemia trait testing

Wednesday, May 8, is celebrated as World Thalassaemia Day. Thalassaemia is a blood related genetic disorder, which includes lack of genes responsible for production of haemoglobin

Updated on: May 08, 2019 05:03 PM IST
Hindustan Times, Pune | By
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In an attempt to avoid birth of children affected with thalassaemia, the thalassaemia society of India, Pune chapter, has proposed mandatory trait test for those who wish to get married, to the state health department.

The severity of the disease depends on the mutations involved in the genes (PICTURE FOR REPRESENTATIONAL PURPOSES ONLY)
The severity of the disease depends on the mutations involved in the genes (PICTURE FOR REPRESENTATIONAL PURPOSES ONLY)

Giving details, Dr Nita Munshi, president of thalassaemia society of India, Pune, said, “We have been conducting thalassaemia screening camps and lectures in colleges since December 2018 and have received a good response so far.”

Wednesday, May 8, is celebrated as World Thalassaemia Day. Thalassaemia is a blood related genetic disorder, which includes lack of genes responsible for production of haemoglobin. The severity of the disease depends on the mutations involved in the genes.

“A child conceived by two thalassaemia minors will be a thalassaemia major. Thalassaemia minor- are carriers, if two thalassaemia minors marry, they have a high chance of producing a thalassaemia major baby. Without a trait test one cannot identify if they’re a thalassaemia minor or not. This blood disorder, which occurs genetically, can be avoided if the parents get their DNAs tested, added Munshi.

Bhaven Parikh, a Symbiosis Centre for Information Technology student who suffers from thalassaemia, said, “It is important for youngsters to get involved in this campaign as marriages between thalassaemia minors can affect the future. Prevention is the only key and hence, tests before getting married should be made compulsory.”

 
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