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.
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.
The Taliban regime has severed Afghanistan's internet connection, isolating millions from the global community in a drastic bid to enforce their strict moral code, with devastating consequences for healthcare, education and livelihoods.
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.
Groundbreaking research from UK scientists revolutionises fertility treatment by transforming skin cells into viable human eggs, offering new hope for infertility and genetic disorders.
The emotional journey of a family who fought for answers after noticing developmental delays in their son, culminating in a rare MICPCH syndrome diagnosis.
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.
Austin police employ groundbreaking DNA technology to identify alleged bicycle thief who left genetic evidence on snack wrapper at crime scene
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.
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.
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.
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.
TV presenter Richard Osman issues a powerful warning about the UK's loneliness crisis, revealing his mother's own heartbreaking struggle and calling for urgent national action.
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.
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.
Groundbreaking data from the HILDA survey exposes a growing loneliness crisis in Australia, with a sharp decline in social connections and community engagement. Discover the causes and concerning trends.
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.
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
Kaavan, the elephant dubbed the 'world's loneliest' after being forced to endure 35 years of heartbreaking isolation in a Pakistani zoo, has died in his Cambodian sanctuary. His story sparked a global campaign for freedom.
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.
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.
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.
A UK school faces backlash after a student was allegedly placed in isolation for wearing the wrong skirt, sparking a heated debate on uniform policies and student rights.
Groundbreaking genetic research brings the dream of resurrecting the extinct dodo bird one step closer to reality. Scientists achieve a major milestone in sequencing its genome, sparking both excitement and ethical debate.
A revolutionary AI system developed by UK researchers can now forecast an individual's genetic risk for over 1000 conditions, transforming preventive healthcare and early diagnosis.
New research from King's College London shows experiencing loneliness as a child may increase dementia risk in later life by 56%, highlighting the long-term impact of early social isolation.
Shocking investigation reveals a New Zealand family's two-decade ordeal of isolation and alleged abuse in a remote wilderness compound, hidden from authorities and society.
Exclusive analysis of Benjamin Netanyahu's controversial 'Super Sparta' doctrine, a radical plan for a besieged, self-reliant Israel that economists warn could trigger severe economic decline and deepen global isolation.
A UK mother's extraordinary bond with her newborn daughter has captured hearts worldwide after the baby was born with an identical facial birthmark. This rare genetic phenomenon defies odds and celebrates the unique beauty of family connections.
World Athletics President Seb Coe calls for a major shift towards genetic and biological testing to create a more robust anti-doping system and ensure a level playing field for all athletes.