Can brushing teeth save from breast cancer?
A study suggests that a bacteria involved in gum disease may silently trigger breast cancer, especially in individuals with a genetic predisposition.
Estonian scientists have discovered why hereditary iron disease is manifested more severely in some cases
Researchers from the University of Tartu have found that symptoms associated with hereditary iron metabolism disorders vary based on specific genetic variants.
Psoriasis: what this genetic disease consists of and why timely diagnosis is key
Dr. Ricardo Galimberti emphasizes the importance of early diagnosis for psoriasis, a genetic disease often misunderstood as a 'nervous' condition.
Union disobeys court decision, and boy with rare disease has been without R$ 90,000 medication for 6 months, says family
A family from Belo Horizonte accuses the Brazilian federal government of not complying with a court order to provide a costly medication for their son, who suffers from a rare genetic disorder.
Scientific Surprise: Mosquitoes Have Been Feeding on Our Blood for 1.8 Million Years
A recent genetic study reveals that certain mosquito species have been feeding on human blood for approximately 1.8 million years.
A Unique Operation is Performed in Kaunas on a Boy from Latvia with a Rare Genetic Disease – Electrodes are Implanted in His Brain
A 10-year-old boy from Latvia with a rare genetic condition has undergone a unique operation in Kaunas to implant electrodes in his brain.
What is neurofibromatosis, the disease that actor Adam Pearson highlighted at the Oscars
The article discusses neurofibromatosis type 1 and its visibility brought by actor Adam Pearson during the Oscars.
What is and how to treat neurofibromatosis, the disease that actor Adam Pearson has
The article discusses neurofibromatosis type 1 (NF1), a genetic disorder highlighted by actor Adam Pearson during the 2026 Oscars, focusing on its effects and treatment options.
Grandmother, sons, and granddaughter - a Sudovian family suffers from a rare Fabry disease
A family from Sudovia faces challenges due to Fabry disease, a rare inherited metabolic disorder.
A Rare Disease and an Irreversible Diagnosis: The Story of Beltrán That Led His Family to Promote a National Law
The story of Beltrán Romero Feris highlights the challenges in diagnosing adrenoleukodystrophy, leading to a national initiative for newborn screening.
Woman 29, took life after losing mum and fearing she had same illness
A 29-year-old woman, Olivia Martinez, took her own life after struggling with the fear of inheriting Huntington's disease, which had claimed the lives of her mother and grandfather.
A 'shield' gene has been found in the global pandemic affecting bananas
Researchers discovered a previously unknown gene in a wild banana that may help save the popular fruit from Fusarium wilt, a destructive global disease affecting Cavendish bananas.
'My son won't survive his teens - being told nothing can be done is a shock'
A mother reveals her shock at her son Frankie being diagnosed with a rare genetic disorder that doctors say is unlikely to allow him to survive past his teens.
Boy with first case of rare genetic disease identified in Brazil arrives in the US for treatment
Eduardo Silva Amaral, the first diagnosed case of hereditary spastic paralysis type 50 in Brazil, has arrived in Dallas, USA, for treatment after raising $2.3 million.
The Hidden Gene: A New Discovery That May Prevent the Extinction of Bananas
A new genetic discovery could help prevent the extinction of the globally dominant Cavendish banana variety, which is threatened by a disease called Fusarium wilt.
‘My rare disease left me blind and obese, it took decades to get a diagnosis’
Rachael Zimbler shares her struggles with Bardet-Biedl Syndrome, a rare genetic condition that led to her blindness and obesity, highlighting the challenges of obtaining a timely diagnosis.
‘Like a spelling mistake’: B.C. teen’s DNA ‘corrected’ to cure rare disease
A B.C. teenager, Ty Sperle, was successfully cured of chronic granulomatous disease through a groundbreaking medical procedure involving genetic correction.
MAARJA KRAIS-LEOSK ⟩ The frequency of kindness towards rare diseases is astounding!
The article discusses the challenges faced by families with rare disease patients in Estonia, highlighting the need for psychological, social, and practical support beyond medical care.
A genetic mutation unleashes a rare disease in Spain and there is no cure: what is fatal familial insomnia?
A genetic mutation is responsible for fatal familial insomnia, a rare neurodegenerative disease predominantly found in Spain, with no known cure and severe implications for those affected.
B.C. man cured of rare disease in world-first for new gene-editing technology
A British Columbia man has become the first person cured of a rare genetic disease through a groundbreaking gene-editing treatment known as prime editing.
Genetic Data, Technological Determinism and Patient Privacy
The article discusses the implications of precision medicine, emphasizing the integration of genetic data and advanced technologies to improve disease prediction and treatment.
Neurofibromatosis: mother and daughter in Paraíba live with a rare disease that spans generations: 'People distance themselves from us, but I entrust it to God'
A mother and daughter from Paraíba, Brazil, are facing the challenges of neurofibromatosis, a rare genetic condition that affects their lives and health.
How cats can provide the key to curing cancer in humans
A detailed genetic map of cancer in domestic cats shows significant similarities with human versions of the disease, potentially guiding new treatment methods for both species.
Promising drug compound attacks fat from genetic roots
A new oral drug compound, TLC-2716, shows promise in significantly reducing blood fat levels linked to fatal heart diseases.
Bread: Health or Disease?
The article discusses the harmful effects of modern processed wheat and gluten on health, linking it to various diseases due to genetic modification and chemical treatments.
The Dilemma of Genetic Testing: Do I Want to Know If I Have Huntington's Disease?
The article discusses the complexities surrounding genetic testing for Huntington's disease, including its implications for individuals and families.
The rare neurogenetic disease where a child's smile hides a diagnosis
The article discusses the rare Angelman syndrome, a genetic condition recognized for its joyful smile but presents significant challenges, particularly in Argentina.
Is mapping a baby's genetic disease risk a healthcare miracle or a step too far?
The article discusses the implications of newborn genomic testing that reveals genetic disease risks, weighing its potential benefits against ethical concerns and psychological impacts.
Chris Hemsworth explained why he hesitated to reveal that he has a genetic predisposition for Alzheimer's
Chris Hemsworth shared his reluctance to disclose his genetic predisposition for Alzheimer's disease, a condition that also affected his grandfather and father.
VLK: Improving cancer disease diagnostics – more tests covered
Since January 1 of this year, genetic tumor tests and PET scans have been reimbursed by the Health Insurance Fund, enhancing the accuracy of cancer diagnoses and treatment selection.
LIFESAVING INNOVATION: Estonia to mass test for severe genetic disease
Starting in 2026, Estonia will offer cystic fibrosis screening to all children born in the country, enabling early treatment and prevention of organ damage.
Grim ‘Celtic Curse’ genetic disease mapped as UK and Ireland hotspots revealed
A new study identifies hotspots in the UK and Ireland for a genetic disease known as the 'Celtic Curse,' which can lead to severe health issues if left untreated.
Doctors: 3 habits can reduce the risk of heart disease more than any medication
Doctors emphasize that practicing three specific habits can significantly lower the risk of heart disease, even more than medication, particularly for those without genetic predisposition.
Sudanese family struggles to treat their son suffering from a rare genetic disease
The article highlights the struggles of a Sudanese family to obtain gene therapy for their son Imad, who is affected by Duchenne muscular dystrophy, a severe rare genetic disorder in children.
Warning signs of rare genetic disease after Jesy Nelson's twins' devastating diagnosis
Singer Jesy Nelson has disclosed that her newborn twins have been diagnosed with spinal muscular atrophy type 1, a severe genetic condition affecting their mobility.
Jesy Nelson says doctors initially dismissed her fears for twin babies
Jesy Nelson shared her heartbreak after doctors overlooked her concerns regarding her twin daughters, who were later diagnosed with a severe genetic disease.
Dane Fathered Two Hundred Children, Transferred Cancer Gene. Slovakia Has No Limit on Offspring from One Sperm Donor
A Danish sperm donor, whose samples were sold across Europe for 17 years, has fathered nearly 200 children, some of whom are fighting cancer due to a rare genetic mutation he carries.