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Scientists have revealed eight healthy babies have been born in the UK using part of a third parent's DNA to reduce their risk of developing mitochondrial genetic diseases. The disease which can lead to children dying at an early age or developing deafness and blindness has no treatment.

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00:00It is a risk reduction strategy. It's very early days. This has been one study and eight babies
00:08have been born and that is a remarkable step forward for the whole field, most importantly
00:13for all of the families out there who have mitochondrial genetic disease. The technique
00:19itself, it's a fairly complex procedure that takes place in an IVF lab where you have a donor
00:26egg with really healthy mitochondria from someone who's donated their eggs and that's a really
00:31important part of this step. Then you have an egg from the mum who has mitochondrial genetic
00:37disease. Take the nuclear DNA from the egg with affected mitochondria and transfer that
00:43nuclear DNA, the DNA that makes us who we are, into the egg with the healthy mitochondria.
00:49So that's how you do it in a lab and members of the team in the UK have been fantastic in
00:54pioneering this technique and moving it from what was a research environment into a clinical
01:01environment and they've really, what they've done in this study has been really remarkable
01:06for the future of genetic disease. There's a really active community that we're waiting
01:12for this in Australia and we're doing our best to get it introduced for them as quickly as
01:17possible so there's quite a few in the, you're waiting for something to be available for them.

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