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HomeHealthDevon woman with rare condition praises genetic testing service

Devon woman with rare condition praises genetic testing service


Anna Varle

BBC South West health correspondent

BBC A woman with a red face and curly brown hair is holding a baby who is dressed in a pink jumperBBC

A woman born with an extremely rare genetic skin condition has two healthy children using a genetic testing service.

A woman born with an extremely rare genetic skin condition has had two healthy children using a cutting-edge genetic testing service.

Georgina Burrough, of Axminster, Devon, has Ichthyosis with confetti, a condition reported in less than 50 people worldwide.

It is characterised by severely dry, red, scaly, and inflamed skin that is highly susceptible to infection and skin cancer.

Ms Burrough said: “We didn’t think having a child was possible without passing on my condition – not a day goes by where I don’t have to pinch myself that these two bundles of joy have been brought into our lives.”

Georgina Burrough A woman in a hospital bed holding a new born baby with her daughter and husband nearbyGeorgina Burrough

Elsie, five, and Annie, seven months, were born using pre-implantation genetic testing

Elsie, five, and Annie, seven months, were born using pre-implantation genetic testing (PGT).

PGT is a type of IVF treatment that involves testing embryos for the condition, allowing couples affected by serious inherited conditions to have an unaffected baby.

The Exeter-based PGT service is the only NHS PGT service in the South West and is run in partnership with Guy’s and St Thomas’ Hospital in London, the UK’s largest PGT provider.

A nitrogen tank is open showing frozen embryos inside

PGT is a type of IVF treatment that involves testing embryos for the condition

Dr Emma Kivuva, consultant clinical geneticist and genetics lead for the service at the Royal Devon University Healthcare NHS Foundation Trust, said: “A small number of cells are removed from the edge of each of the developing embryos and we test these cells using a test we have designed for the family’s specific genetic condition.

“We would then only transfer an unaffected embryo into the womb.”

Aga Kowalska Photography A family portrait showing a mum dressed in an oatmeal cardigan and white shirt with a baby in a white baby grow, a girl in a white top and a man in a white shirtAga Kowalska Photography

The condition Georgina has has a 50% risk of being passed down to any children

Ms Burrough’s condition had a 50% risk of being passed down to any children, and some babies are so profoundly affected that they do not survive.

“I have to undergo a lot of treatment every day, which takes three to five hours and involves bath emollients, creaming and exfoliating,” she said.

“I don’t regulate my body temperature.

“I wouldn’t be able to cope with knowing I had passed on the condition.”

Annie is the 50th baby born to this service in Exeter.

She said she hoped telling her story would open the doors for other people in similar situations and people would feel able to give it a go.

A woman with brown short hair and glasses in a clinical setting.

Dr Emma Kivuva, consultant clinical geneticist, said the treatment was accessible to people in the South West

Dr Emma Kivuva, consultant clinical geneticist and genetics lead for the service at the trust, said: “We are extremely proud to have marked the milestone of the 50th baby born thanks to the PGT service.

“By offering this service, we can help families who might otherwise face difficult decisions about having children due to their genetic risk.

“Providing a service in the South West makes treatment more accessible to people living in this region.”

Dr Sonal Paradkar, PGT co-ordinator for the clinic said, said service could cater for several thousand rare genetic conditions.

These include Huntington’s disease, cystic fibrosis and some rare inherited cancer conditions.



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