New Alzheimer's Gene Discovered in High-Risk Americans
Groundbreaking research reveals a previously unknown gene variant that dramatically increases Alzheimer's risk, offering new hope for early detection and treatment strategies.
Category : Search result: genetic predisposition
Ancient DNA Rewrites Aztec Origins Story
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.
Britain's only patient with ultra-rare disease
Exclusive story of Dean Sims, the solitary UK case of Mandibuloacral Dysplasia, and his extraordinary journey through the healthcare system.
Study: Intense Exercise May Increase MND Risk
Groundbreaking research from the University of Sheffield suggests vigorous exercise may accelerate motor neurone disease onset in those with predisposing genes, challenging fitness norms.
DNA Database Controversy Sparks Privacy Concerns
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.
Diabetes gene breakthrough could transform treatment
Groundbreaking research reveals how a specific gene disrupts insulin production in the pancreas, offering new hope for millions living with diabetes worldwide.
MAFS Emma Barnes reveals heartbreaking IVF journey
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.
Women genetically more vulnerable to depression - study
Groundbreaking research uncovers significant genetic differences that make women more vulnerable to depression, challenging long-held assumptions about mental health gender disparities.
EastEnders Star Reveals Son's Rare Condition Struggle
EastEnders actress Kellie Bright opens up about her family's emotional journey navigating her son's rare genetic disorder and the daily challenges they face.
Alien DNA Found in Humans? Study Reveals Genetic Evidence
Shocking new scientific research proposes that humanity's genetic blueprint contains evidence of extraterrestrial manipulation, challenging everything we know about human evolution.
46-year Florida kidnapping cold case solved
After nearly five decades of silence, Florida authorities have finally identified the perpetrator in Susan Perkins' shocking 1978 kidnapping case, bringing long-awaited closure to her grieving family.
Cousin marriages and substance abuse drive infant deaths
Groundbreaking ONS statistics expose how parental consanguinity and substance abuse are contributing to tragic infant deaths across Britain, with experts calling for urgent public health intervention.
Baby's rare disease battle: Family's 5-month diagnosis wait
A UK family shares their emotional journey as their newborn son battles a rare neonatal disease, facing months of uncertainty and fighting for answers in the NHS system.
Mark and Rebecca Black: The Siblings Who Married
Exclusive investigation reveals how Mark and Rebecca Black, raised as brother and sister in Scotland, discovered they were biological parents and entered into a secret marriage that stunned their community.
Scientists create human eggs from skin cells in fertility breakthrough
Groundbreaking research from UK scientists revolutionises fertility treatment by transforming skin cells into viable human eggs, offering new hope for infertility and genetic disorders.
Toddler's mystery illness diagnosed as rare genetic disorder
The emotional journey of a family who fought for answers after noticing developmental delays in their son, culminating in a rare MICPCH syndrome diagnosis.
NHS expands cancer screening for Angelina Jolie gene women
Thousands of British women carrying the BRCA1 gene mutation face increased ovarian cancer risk. New NHS programme offers regular blood tests to detect early signs.
DNA on snack wrapper helps police identify bike thief
Austin police employ groundbreaking DNA technology to identify alleged bicycle thief who left genetic evidence on snack wrapper at crime scene
Mother's battle against daughter's ultra-rare GRIN1 disease
Exclusive: The heart-wrenching story of a mother's battle to save her daughter, Arianna, from the ultra-rare GRIN1 gene mutation, a condition so uncommon it affects just a handful of people globally.
Huntington's Disease: New Drug Slows Progression in Trial
A revolutionary new drug, pridopidine, has shown significant promise in slowing the progression of Huntington's disease, offering new hope to UK families affected by the genetic condition.
Huntington's Disease Breakthrough: Revolutionary Therapy Offers Cure Hope
Groundbreaking medical research from UCL and University College London Hospitals has successfully lowered levels of the toxic protein that causes Huntington's disease using an innovative genetic therapy injected into the spinal fluid.
Baby Born Without Eyes in Ultra-Rare Genetic Condition
The parents of a baby girl born without eyes due to an incredibly rare genetic condition share their emotional journey and determination to give their daughter the best life possible.
Ancient Irish DNA Study Rewrites History Books
Groundbreaking research from Queen's University Belfast uncovers the true genetic origins of the Irish people, tracing ancient DNA back to mass migrations from the Middle East and Eastern Europe.
Son's Rare Disorder Destroys Home: Mother's Plea for Help
An East Sussex mother's heart-wrenching account of her son's ultra-rare GRIN2B condition, which causes extreme violence, property destruction, and a desperate fight for support.
Turkana People's Genetic Adaptation to Harsh Environment Revealed
Groundbreaking study reveals the remarkable genetic adaptations of the Turkana people, offering new insights into human evolution and survival in one of Africa's most unforgiving landscapes.
Routine blood test reveals incurable genetic condition
Jade, 33, went for a routine blood test expecting nothing unusual. Weeks later, she received a life-altering diagnosis of Hereditary Angioedema (HAE) - a rare genetic disorder with no cure. Her story highlights the importance of recognising unusual sympto
British DNA study transforms African ancestry understanding
A landmark study from the Natural History Museum reveals how British DNA is reshaping our understanding of African genetic history, uncovering centuries of migration and diversity.
Genetic breakthrough targets Africa's malaria mosquito
Scientists crack the genetic code of the Anopheles funestus mosquito, a major malaria vector in Africa, paving the way for innovative genetic control strategies to combat the deadly disease.
Teen's decade-long battle with agonising sickle cell disease
Exclusive: A teenager's life has been defined by unimaginable pain and hospital isolation due to the cruel genetic condition sickle cell disease, robbing her of a normal childhood and future dreams.
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