A breakthrough NHS study reveals whole-genome sequencing provides diagnoses for rare genetic conditions two years earlier, offering families crucial answers and access to care. Read the inspiring story of three-year-old Nathaniel.
A breakthrough NHS study reveals whole genome sequencing is diagnosing rare genetic conditions in children two years sooner, transforming care for families like Nathaniel's in London.
At 26, Caitlin Magagna battles cystic fibrosis, an invisible genetic condition. Her story reveals the high costs and daily struggles, offering hope with new treatments. Discover her journey.
Coronation Street actress Samia Longchambon opens up about living with Raynaud's disease for two decades. Discover her coping tips and how she manages the circulation condition.
Leading scientists refute claims that gut bacteria cause autism, urging a shift in research focus towards genetics. Discover the facts behind the debate.
Rugby league star Mark Riddell breaks down discussing daughter Ava's Ogden Syndrome, affecting just four children in Australia. Read his inspiring family story.
A Swansea mum is in a desperate race against time after her four-year-old son Tate was diagnosed with Sanfilippo Syndrome, a rare and terminal childhood dementia.
In an extraordinary medical breakthrough, 19-month-old Oscar Sparrow from West Midlands has been identified as the only person worldwide living with a never-before-seen genetic mutation, offering new hope for rare disease research.
A mother reveals how her daughter endured cruel bullying for years before doctors discovered her weight struggles were caused by rare Bardet-Biedl syndrome, exposing the hidden reality of genetic disorders.
BBC Countryfile presenter Adam Henson opens up about his daughter's genetic condition diagnosis and how it's changed his family's perspective on life and farming.
Groundbreaking research reveals new method to identify cancer-causing genetic changes early, potentially revolutionising preventative care and saving thousands of lives through timely intervention.
The heartbreaking story of Isabelle Tate, a young girl from England fighting Charcot-Marie-Tooth disease, a rare genetic condition threatening her ability to walk and enjoy a normal childhood.
Isabelle Adora Tate's courageous battle against a devastating neurological condition ends at just 21, as her grieving mother pays emotional tribute to her 'beautiful warrior' daughter.
Exclusive: The heartbreaking story of a family coping with their daughter's rare Cri Du Chat syndrome, revealing the daily challenges and emotional toll of caring for a child with complex needs.
A Hampshire woman developed Foreign Accent Syndrome after suffering a stroke, causing her to speak with a Thai accent despite never visiting Thailand. Medical experts explain this rare neurological condition.
Exclusive: Mother's emotional journey as her son battles rare chromosome disorder and the family's desperate search for answers in the UK healthcare system.
Jade Millner shares her emotional story of losing two babies to Patau's syndrome and her campaign for better baby loss support in the UK healthcare system.
Singer Anne-Marie opens up about her young son's harrowing health journey with a rare genetic disorder, sharing emotional details about hospital stays and the impact on family life.
The NHS is rolling out a groundbreaking genetic testing programme to identify thousands of Britons with undiagnosed hereditary haemochromatosis - a dangerous iron overload condition that can cause organ damage if untreated.
An investigative journey into the lives of the Whittakers, known as America's most inbred family, uncovering their isolated existence and the genetic consequences of generations of intermarriage.
Revolutionary xenotransplantation procedure offers new hope for thousands on organ waiting lists as scientists achieve unprecedented success with genetically engineered pig liver supporting human patient.
In a world-first medical breakthrough, surgeons have successfully attached a genetically modified pig liver to a human patient, potentially revolutionising organ transplantation and tackling donor shortages.
Groundbreaking research reveals a previously unknown gene variant that dramatically increases Alzheimer's risk, offering new hope for early detection and treatment strategies.
Groundbreaking genetic research reveals the astonishing origins of the Aztec civilization, tracing their ancestors' epic 1,000-mile migration from Mexican deserts to their eventual empire.
Exclusive story of Dean Sims, the solitary UK case of Mandibuloacral Dysplasia, and his extraordinary journey through the healthcare system.
Groundbreaking research from the University of Sheffield suggests vigorous exercise may accelerate motor neurone disease onset in those with predisposing genes, challenging fitness norms.
Conservative commentator Charlie Kirk's alarming claim about Utah's DNA collection practices sparks debate over genetic privacy rights and government overreach in criminal investigations.
Groundbreaking research reveals how a specific gene disrupts insulin production in the pancreas, offering new hope for millions living with diabetes worldwide.
Married at First Sight favourite Emma Barnes opens up about her devastating fertility struggles and genetic condition discovery while trying for a baby with husband Matt.
Groundbreaking research uncovers significant genetic differences that make women more vulnerable to depression, challenging long-held assumptions about mental health gender disparities.