THREE CHILDREN who have all been affected by an unexplained kidney disease have finally been given answers.

Siblings Noah, 23, and Ariel, 19 have both had kidney transplants and their younger brother, Casper, 15, has been diagnosed with kidney disease.

The Bingham family, from Hexham, Northumberland, are part of the Genomics England 100,000 Genomes project and were one of the families identified as having the gene deletion, NPHP1-related kidney failure.

Noah presented with kidney failure just after finishing his A-levels and, at the same time, Ariel was being treated for reduced kidney function.

Both now have donated kidneys as their own organs function reduced to dangerously low levels. Sadly, Noah’s transplanted kidney failed after only 16 months, and he had to start haemodialysis again in February this year.

Mum Sarah, 51, a home educator, said: “The genetic tests carried out by Professor John Sayer and his team allowed Casper to receive his diagnosis before he was symptomatic.

“The knowledge that Casper will go into kidney failure and eventually need a transplant, though overwhelming at times, has meant that we can arrange the support he needs and help him prepare for surgery and treatments well before they are necessary.

“When nobody is able to explain why your children are ill, it is very unsettling, with no means of clarifying what might happen in the future. The diagnosis has meant that we have been able to prepare ourselves for the medical issues our children face.

“It’s great that this research is being carried out at Newcastle University as it means patients with the condition can get a better understanding of their medical needs and hopefully new treatments may be developed in the future thanks to the research that is being done.” 

Sarah and husband, Darryl, 52, a chartered building surveyor, have been strong advocates for kidney patients and work with Kidney Research UK to help support patients.

Scientists say that as this missing gene has now been identified, and mutations within it found, they have been able to classify this as NPHP1-related kidney failure.

Professor John Sayer, Deputy Dean of Biosciences at Newcastle University, said: “Our new genomic methods and their results has huge implications for the patients and families with kidney failure who were previously genetically unsolved.

“What we are now able to do is give some patients a precise diagnosis, which allows their investigations, treatment and management to be tailored to their needs for the best possible outcomes.

"We knew that many of our unsolved cases had a genetic disorder, and this new approach enables us to solve these cases definitively.

“We can now give an accurate genetic diagnosis to many more families affected by kidney disease and our hope is to provide a proper diagnosis for many more families in the future.

“This work is a reminder that it is always worth investigating the underlying reasons for kidney failure to get to the bottom of the condition.

“Finding a genetic cause of kidney failure has huge implications for the patient and also for other family members, especially if they are wishing to donate a kidney to their loved one.”