DNA test reveals shocking paternity secret after 50 years
A woman's life was turned upside down after a DNA test revealed her father wasn't biologically related to her. Read her emotional journey of discovery.
Category : Search result: genetic engineering
Toddler’s fever was rare genetic illness—£500K treatment needed
A toddler initially treated for a fever was later diagnosed with a rare genetic illness. Doctors now hope a £500,000 treatment can slow the disease's progression.
Genetic clues to chronic fatigue syndrome discovered
New research reveals potential genetic markers linked to chronic fatigue syndrome, offering hope for better diagnosis and treatment.
Eiffel Tower grows taller in summer heat
Paris's iconic Eiffel Tower expands by up to 15cm during hot weather due to thermal expansion, a fascinating quirk of physics.
Genetic study reveals clues to Chronic Fatigue Syndrome
A groundbreaking study has identified key genetic markers linked to Myalgic Encephalomyelitis (ME/CFS), offering new hope for understanding this debilitating condition.
Italy approves world's longest suspension bridge
Italy has greenlit the construction of the world's longest suspension bridge, connecting Sicily to the mainland in a historic infrastructure project set to transform travel and boost the economy.
Aaron Chalmers' son diagnosed with rare Apert Syndrome
Former Geordie Shore star Aaron Chalmers and his ex-partner Talia Oatway reveal their son Oakley's battle with Apert Syndrome, a rare genetic condition.
Genetic clues to chronic fatigue syndrome uncovered
Scientists have identified key genetic markers linked to chronic fatigue syndrome, offering new hope for diagnosis and treatment.
Inside America's Most Inbred Family
A journalist recounts their unsettling encounter with the Whittaker family, known as one of America's most inbred families, revealing their struggles and the harsh realities of genetic isolation.
Rare condition means some people never feel hungry
A rare genetic condition means some individuals never experience hunger, leading to unique health challenges and lifestyle adjustments. Discover their fascinating stories.
David Suchet on grandson's rare genetic disorder battle
Actor David Suchet shares his family's journey with tuberous sclerosis, a rare genetic condition affecting his grandson, to raise awareness and support research.
David Suchet on grandchild's tuberous sclerosis diagnosis
Renowned actor David Suchet shares his family's journey with tuberous sclerosis, advocating for greater awareness and research into the rare genetic condition.
David Suchet's grandson battles rare genetic disorder
Beloved actor David Suchet reveals his grandson's battle with a rare genetic disease, sharing the family's emotional journey and raising awareness for the condition.
Family's heart attacks reveal genetic health risk
A family's terrifying ordeal with heart attacks has prompted vital health checks, revealing a hidden genetic condition.
Baby's 'colic' diagnosed as rare fatal disease
A baby boy's persistent crying was dismissed as colic before a devastating diagnosis revealed a rare genetic disorder. His parents share their emotional story.
Rolls-Royce's high-flying turnaround faces long-term test
Rolls-Royce's impressive turnaround under CEO Tufan Erginbilgic has investors buzzing. But can the company maintain this turbocharged performance for the long haul?
MyHeritage DNA Test Kit Review: Explore Your Ancestry
Discover how the MyHeritage DNA test kit can help you explore your genetic roots with detailed ethnicity estimates and family matching features.
Dad's tearful TV revelation about daughter's rare illness
A father emotionally shares his family's struggle with his daughter's rare genetic disorder during an appearance on ITV's This Morning, raising awareness and touching viewers' hearts.
Hamilton's engineer Bono in shock Ferrari talks
Lewis Hamilton's trusted race engineer Peter Bonnington, known as 'Bono', is reportedly in talks to join Ferrari, marking a major shake-up in F1's engineering landscape.
Sydney Uni appoints first female engineering dean
The University of Sydney has made history by appointing its first female dean of engineering, marking a significant step towards gender equality in STEM leadership.
Genetic secret of people who never caught COVID revealed
Groundbreaking research reveals why certain individuals avoided COVID-19 infection entirely, pointing to a remarkable genetic advantage that kept them safe.
Mum's 999 call as son denied hospital bed
A mother's harrowing 999 call reveals the NHS crisis as her 12-year-old son with a rare genetic disorder is left without a hospital bed for days.
Genetic test predicts obesity risk decades in advance
A revolutionary genetic test may soon predict obesity risk years before symptoms appear, offering hope for early intervention and prevention.
Mother solves daughter's rare genetic disorder mystery
After years of uncertainty, a determined mother finally uncovers the truth behind her daughter's baffling health condition—a rare genetic disorder that had eluded doctors for years.
DNA test predicts childhood obesity risk
A groundbreaking DNA test may soon help identify children at risk of obesity early, offering parents and doctors a chance to intervene before health issues arise.
Mitochondrial donation IVF: UK's genetic breakthrough
The UK's groundbreaking mitochondrial donation IVF technique marks a significant but careful step in genetic innovation, offering hope to families affected by mitochondrial diseases.
NASA Tests Quiet Supersonic X-59 Jet
NASA's groundbreaking X-59 supersonic aircraft promises to bring back commercial supersonic flights without the disruptive sonic booms. Discover how this marvel of engineering could change aviation forever.
UK approves three-parent IVF to prevent genetic diseases
The UK has become the first country to officially approve a groundbreaking IVF technique that incorporates DNA from three individuals, aiming to prevent genetic disorders in babies.
IVF Breakthrough: Eight Babies Born Free of Mitochondrial Disease
A groundbreaking IVF procedure has successfully prevented mitochondrial disease in eight babies, marking a significant milestone in genetic medicine.
Mother's plea after daughter dies from rare disease
A grieving mother shares her devastating story after losing her daughter to mitochondrial disease, a rare and often misunderstood condition.
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