A new Channel 4 documentary uncovers Hitler's Kallmann Syndrome through DNA analysis, explaining his mysterious behaviour and relationships. Discover the shocking genetic truths behind the dictator.
New DNA analysis of Adolf Hitler confirms a genetic disorder affecting his sexual development and suggests neurodiverse conditions. Read the full story on the Channel 4 documentary findings.
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.
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.
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.
Groundbreaking research from The Institute of Cancer Research reveals men with BRCA2 gene faults face dramatically higher prostate cancer risks. Experts call for urgent screening changes.
Groundbreaking research reveals men carrying the BRCA 'Angelina Jolie gene' face dramatically higher prostate cancer risks and require annual screenings for early detection.
A decades-old murder mystery in Columbia, South Carolina has been solved through groundbreaking DNA analysis, leading to the identification of a suspect who died years ago.
A major breakthrough in the notorious Long Island serial killer investigation reveals DNA evidence has identified a suspect in the 1993 murder of Sandra Costilla, potentially cracking one of America's most enduring cold cases.
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.
A groundbreaking NHS screening programme is now detecting Tyrosinaemia Type 1 in newborns just 24 hours after birth, preventing life-threatening complications through early intervention.
Groundbreaking research reveals how genetic testing could transform treatment for deadly blood cancer multiple myeloma, offering personalised therapy approaches.
Exclusive: A grieving sister's powerful account of losing two siblings to sickle cell disease reveals shocking gaps in NHS care and demands urgent government action.
Two-year-old Ivy's constant hunger battles a rare genetic disorder called Prader-Willi syndrome, leaving her parents in a 24/7 vigil against life-threatening complications.
New research uncovers how children may inherit their parents' cognitive decline patterns, with significant implications for dementia prevention and early detection strategies in UK families.
British scientists pioneer revolutionary gene therapy treatment showing remarkable results in children suffering from debilitating SYNGAP1 syndrome, a rare genetic condition causing severe autism, epilepsy and developmental delays.
Groundbreaking genetic research uncovers surprising Roman and Latin heritage in New Orleans residents, challenging conventional understanding of the city's European roots.
Groundbreaking forensic science cracks one of Britain's most perplexing cold cases, bringing closure to families after four decades of uncertainty.
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.
Sir Ian Wilmut, the pioneering scientist who failed biology at Eton but went on to lead the team that cloned Dolly the Sheep, has passed away aged 92. Discover the remarkable journey of the man once told his scientific dreams were 'ridiculous'.
Chinese scientists achieve revolutionary medical breakthrough as modified pig liver sustains brain-dead human body for 72 hours, potentially solving organ transplant shortages
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.