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.
New DNA analysis reveals Adolf Hitler had Kallmann syndrome, a rare genetic condition impacting puberty. Discover the findings and what it means.
Relly Ladner was told she might never walk again after Guillain-Barré syndrome. Defying odds, she now runs marathons. Read her incredible recovery journey.
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.
The devastating story of Sarah, a mother with rare dementia who can no longer recognise her own children, as her family fights for access to revolutionary treatment that could save her.
A mother's terrifying ordeal as her healthy son suddenly develops rare neurological condition ADEM, sparking urgent NHS investigation into childhood illness.
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.
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.
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.
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.
A Hampshire woman developed Foreign Accent Syndrome after suffering a stroke, causing her to speak with a Thai accent despite never visiting Thailand. Medical experts explain this rare neurological condition.
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.
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.
The Biden administration makes unprecedented investments in Western rare earth companies to secure critical minerals and challenge China's market dominance in green technology.
Groundbreaking research from Stanford University has identified the biological reason women face higher dementia risk. The X chromosome connection explained.
A young woman from Manchester lives in constant pain with a rare condition that causes her ribs to dislocate when she laughs, coughs or even breathes deeply, leaving her unable to work or enjoy simple pleasures.
Discover how a rare 2009 Kew Gardens 50p coin hiding in your pocket change could be worth a small fortune to collectors.
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.
In an extraordinary medical case, Lisa Millar from Largs, Scotland, awoke from a two-week coma speaking fluent French despite barely remembering the language since school. Doctors are baffled by this rare phenomenon of Foreign Accent Syndrome.
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.
Popular YouTuber Alfie Deyes reveals his shocking diagnosis with a rare swallowing condition called eosinophilic oesophagitis after suffering for years with what doctors thought was acid reflux.
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 emotional journey of a family who fought for answers after noticing developmental delays in their son, culminating in a rare MICPCH syndrome diagnosis.
Discover how four rare 50p coins featuring iconic British designs could be hiding in your pocket change, with collectors paying hundreds of pounds for these sought-after pieces.
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.
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.
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.
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
A seemingly healthy mother-of-two's legs suddenly failed, leading to a terrifying medical mystery and a rare diagnosis that changed her life forever.
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 seemingly ordinary 1p coin, minted with a unique error in 1983, has just sold at auction for a staggering £127,000, making it one of the most valuable modern coins in the UK.