Delegates at the European Society of Human Reproduction and Embryology heard that the team have so far successfully identified the male or Y chromosome from the foetus in the mother's blood, proving their technique works. It can be used as early as 6(six)-to-8(eight) weeks, they said.
"...It is the holy grail of prenatal diagnosis to try and find a reliable method of diagnosing Down's syndrome and other chromosome abnormalities without doing invasive testing.."
Study leader Dr Suzanna Frints, a clinical geneticist at Maastricht University Hospital, says the costs of such tests are coming down all the time and it could eventually be available for as little as £25.
"Blood samples can be taken during routine antenatal visits." "It is inexpensive compared to the costs of invasive prenatal diagnosis, and could easily be implemented at low cost." She added: "At the moment, the reliability of the test is about 80% due to false negative results, but we are working to improve the accuracy."
Professor Stephen Robson, spokesman for the Royal College of Obstetricians and Gynaecologists, said there are a number of labs around the world working on different techniques for such diagnostic tests.
"It is the holy grail of prenatal diagnosis to try and find a reliable method of diagnosing Down's syndrome and other chromosome abnormalities without doing invasive testing."
"This is another technique that could offer the potential to diagnose Down's syndrome non-invasively but it's important to emphasise that it is some years away."
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