The 'three-parent' technique allows parents with rare genetic mutations to have healthy babies.
The boy's mother carries genes for Leigh syndrome, a fatal disorder that affects the brain, muscles and nerves of developing infants. Genes for the disease reside in DNA in the mitochondria, which provide energy for our cells.
The parents of the baby, a Jordanian couple, had been trying to start a family for almost 20 years.
In 2005, the couple gave birth to a baby girl. Their daughter was born with Leigh syndrome, and died aged six.
The couple's second child had the same disorder, and lived for 8 months, the 'New Scientist' reported.
The couple sought out the help of John Zhang and his team at the New Hope Fertility Centre in New York City.
Zhang used an approach called spindle nuclear transfer. He removed the nucleus from one of the mother's eggs and inserted it into a donor egg that had its own nucleus removed.
Zhang's team used this approach to create five embryos, only one of which developed normally. This embryo was implanted in the mother and the child was born nine months later on April 6, this year.
When researchers tested the boy's mitochondria, they found that less than one per cent carry the mutation.
This may be too low to cause any problems; generally it is thought to take around 18 per cent of mitochondria to be affected before problems start, researchers said.
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