A two-year-old British girl is battling an aging disease so rare she’s thought to be only affected individual in the world.
Isla Kilpatrick-Screaton, from Leicester, England, has the so-called “Benjamin Button disease” mandibuloacral dysplasia, which causes her cells to age far too quickly.
Just 40 cases of the genetic condition have ever been reported, according to the National Organization for Rare Disorders.
DNA tests reveal Isla carries a specific mutation that has never before been seen in any other sufferer.
With her condition so rare, the toddler — who battles a heart disorder and breathing difficulties — faces an uncertain future.
Isla’s mother, Stacey Kilpatrick-Screaton, 33, enjoyed a normal pregnancy until she went into early labor at 36 weeks on Feb. 2, 2017.
The delivery was dramatic, with the baby nearly suffocating.
“Once she was born and [they] cut off the umbilical cord, she couldn’t keep her oxygen level above 60 percent, when it needed to be 90 percent,” Kilpatrick-Screaton, who is Isla’s full-time carer, said.
“The nurses were trying to keep her airways open for what felt like hours. We expected to be able to see her but she was taken to neonatal intensive care.
“We nearly lost her. She was fighting against everything they were trying to do.”
Isla was put in an induced coma for the first five days of her life, with her parents unable to hold her.
A month after she was born, the youngster was deemed well enough to go home, but the good news didn’t last long.
“We had to ring an ambulance after six days because she started choking, spluttering and turning blue when we were bottle-feeding her,” said Kilpatrick-Screaton, who is also mother to 7-year-old Paige.
“One of us would do CPR while the other held the phone.
“In the hospital they managed to clear her airways and she spent another two weeks there.”
At 3 months, she was rushed back when her tongue blocked her airway, causing her to turn blue. After being resuscitated, doctors discovered this happened every time she got upset.
Following numerous tests, Isla was eventually diagnosed with mandibuloacral dysplasia in October 2017.
Baffled, the youngster’s parents were reportedly told to look up the disorder online, with doctors unable to explain exactly what was wrong.
“We were lightheartedly told to 'get Googling,’” Kilpatrick-Screaton said.
More than two years on, the parents still feel clueless about their daughter’s condition.
“We're told her condition isn't life-limiting but we just don't know for sure as her case is so unique,” dad Kyle Kilpatrick-Screaton, 36, said.
“We have been left in the dark somewhat. There's not really any support available so we just take it day by day.”
The 2-year-old, who is fed via a tube, weighs just 15 lbs. and has only recently started crawling. Barely able to speak, she largely communicates via sign language.
“Isla makes herself understood and is very clever,” her mom said. “She is very expressive and communicative”.
The condition has affected the youngster in a variety of other ways.
“Her symptoms are narrow airways; pale, thin skin and a small jaw which means her tongue is far back in her throat which can stop her breathing,” Kilpatrick-Screaton said.
“She is either cold or red-hot. If she becomes badly unwell her temperature can go up to 40°C (104°F).
“She sees about 12 consultants, has from 1-6 appointments a week and a whole cabinet of medical records.”
The family rely on the Rainbows Childrens’ hospice, in Loughborough, to let Isla play like any other child.
“It is just amazing being able to see Isla playing with her sister with her mum nearby,” her dad, a self-employed builder, said.
The family are speaking out to help others learn about their daughter’s disease.
“I just really want to raise awareness of the disease to help Isla and other children that might have it in the future,” he said.
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