UK boy is only person in world with deadly condition
Oli-Jay Morris, 2, is the only known person with a unique gene mutation. His family are fundraising £14,000 for a personalised treatment plan to save his life.
Category : Search result: rare genetic mutation
Sisters, 27, diagnosed with breast cancer months apart
Two North Carolina sisters in their 20s, both carrying the CHEK2 gene mutation, were diagnosed with breast cancer within months of each other, prompting urgent double mastectomies. Their story underscores the critical need for early genetic screening.
Rare Pink Grasshopper Found in New Zealand
A stunning pink grasshopper, an exceptionally rare genetic variant, has been discovered during a survey in New Zealand's Mackenzie Basin. Discover the story behind this unique insect.
Rare Pink Grasshopper Discovered in New Zealand
An incredibly rare pink grasshopper, a genetic marvel, has been found in New Zealand's Mackenzie Basin. Discover the story behind this unique insect and its fight for survival.
Mark Riddell's tearful reveal about daughter's rare disease
Rugby league star Mark Riddell breaks down discussing daughter Ava's Ogden Syndrome, affecting just four children in Australia. Read his inspiring family story.
Hitler's rare genetic sexual disorder uncovered
New DNA analysis reveals Adolf Hitler had Kallmann syndrome, a rare genetic condition impacting puberty. Discover the findings and what it means.
Boy, 4, diagnosed with rare childhood dementia
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.
UK toddler first in world with unique genetic condition
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.
Bullied for weight: Teen's rare genetic disorder revealed
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.
Cancer detection breakthrough spots genetic risks early
Groundbreaking research reveals new method to identify cancer-causing genetic changes early, potentially revolutionising preventative care and saving thousands of lives through timely intervention.
Human Evolution Accelerates in Unprecedented Ways
Groundbreaking research reveals humans are evolving in ways never seen before, with natural selection actively shaping our genomes and removing harmful mutations at an accelerating pace.
Child's battle with rare disease stealing her ability to walk
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.
Teen's death from rare Charcot-Marie-Tooth disease
The heartbreaking story of Isabelle Tate, a vibrant teenager whose life was cut short by the little-known genetic condition Charcot-Marie-Tooth disease, sparking urgent calls for greater awareness and research funding.
Daughter's rare condition breaks hearts daily
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.
Rare 50p Coin Sells for £113 at Auction
A scarce 2009 Kew Gardens 50p coin has sold for over double its face value in a recent auction, sparking renewed interest in coin collecting across the UK.
Aaron Chalmers' son hospitalised with rare disorder
Former Geordie Shore personality Aaron Chalmers reveals his young son Oakley faces unexpected hospital procedure while battling rare genetic condition that requires ongoing medical care.
New mpox strain detected in Los Angeles
Health officials sound alarm as dangerous new mpox variant emerges in California, raising concerns about global spread and vaccine effectiveness.
Mum's heartbreak as son battles rare chromosome disorder
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.
US Bets Big to Break China's Rare Earth Monopoly
The Biden administration makes unprecedented investments in Western rare earth companies to secure critical minerals and challenge China's market dominance in green technology.
Anne-Marie reveals son's rare genetic condition diagnosis
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.
NHS screens thousands for hidden genetic disorder
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.
Rare 50p Coin Could Be Worth Over £500
Discover how a rare 2009 Kew Gardens 50p coin hiding in your pocket change could be worth a small fortune to collectors.
Girl's constant hunger battle with rare genetic condition
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.
America's Most Inbred Family: The Whittaker Story
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.
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.
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.
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.
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.
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.
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