'Our son wouldn't laugh or sit up before rare diagnosis'

'Our son wouldn't laugh or sit up before rare diagnosis' Bertie, aged five, was diagnosed after his parents noticed he wasn't hitting his milestones A five-year-old boy has been diagnosed with an exceptionally rare genetic condition after his parents noticed he wasn't "laughing or sitting up". Bertie Napier Roberts was diagnosed with Beta-propeller Protein-associated Neurodegeneration (BPAN) at the age of four. BPAN is a rare condition triggered by mutations in the WDR45 gene on the X chromosome, resulting in an accumulation of iron in the brain that causes cognitive deterioration in adulthood. Boys typically experience more severe symptoms than girls due to the absence of an additional X chromosome. Should Bertie reach the second stage of the disease, he faces the prospect of developing dementia, Parkinson's and dystonia. His family is hopeful that he can receive gene therapy replacement treatment at Great Ormond Street Hospital, provided funding for the trials can be secured. Emiliee, a stay-at-home mum from Canterbury, Kent, said: "My head was spinning when he was diagnosed - I burst into tears. How awful for him - I was a mess. "The downside is the second degree of the disease is dementia, Parkinson's and loss of life. There are fewer than 500 cases in the world and only 10% are boys, because girls have two X chromosomes, so they have one healthy gene. "Whereas boys, their X chromosome is broken, so it shouldn't have been a possibility in the first place. He is a massive miracle to us all. "He makes little to no protein whatsoever to recycle brain cells, so they then die and your body naturally produces iron, which then accumulates in his brain and causes the second-degree stage. Mobility wise he can shuffle, but can't walk or speak. "If this gene therapy isn't made by the time he does hit the second degree he's going to lose all those skills - even smiling. It's what he uses to reassure us and that's my biggest fear, waking up and not seeing him smile." Bertie is Emilee's fourth child, so she and Grant Roberts, 32, knew immediately that he wasn't reaching his developmental milestones. She told Sell Us Your Story: "At nine months old I got hold of the health visitor and I thought it was maybe autism at that point - I didn't think about a genetic disease or anything like that. He failed his nine-month check and she said she thought he had global development delay. "We saw a paediatrician and physio. They were trying to get him to move and he was quite stiff on his right side. "He used to daydream a lot and he would go into a daze mid-play. The physio asked how often he did that and they said they thought he was having absent seizures." Bertie was subsequently diagnosed with absent seizures and global development delay, and underwent genetic testing. The initial results came back clear, prompting doctors to carry out a full sequencing — leaving Emilee and Grant facing an agonising year-long wait for the outcome. The results ultimately revealed a mutated WDR45 gene, and Bertie was subsequently diagnosed with BPAN by a specialist at Great Ormond Street Hospital, which is actively researching the condition. Upon receiving the full genetic testing results, Emilee began conducting her own research into BPAN. She explained: "We got a phone call and they basically said they had found a mutated WDR45 gene. I looked into and I put his mutation gene variant into Google - it came up with BPAN. "I looked into that more and everything was ticking boxes for me. I contacted the neurologist and said I think he has this. "It's usually an automatic BPAN diagnosis if he has that mutation - she hadn't heard of it before. I got hold of a specialist professor at GOSH and by February she'd seen us and gave us the diagnosis." The next step for Bertie and his family will be gene therapy, which they hope will halt the disease from advancing to its second stage. Emilee added: "Gene therapy is there to stop the second degree happening - the second degree is when they start getting too much iron build-up. They are doing vital research at GOSH and human trials are the next step. "The Action for BPAN charity is trying to raise £2.3M to fund that by 2027. For kids with BPAN it's not managed with medication- it's the unmanageable epilepsy which scares me. The anxiety I have every morning going in there and not knowing if he's okay or not." You can support Bertie via GoFundMe.