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6691 results for "disease diagnosis"
A new AI algorithm called EvORanker is ending the decade-long "diagnostic odyssey" for families with rare diseases, identifying the correct disease-causing gene in 70% of test cases. The tool looks across evolution to spot hidden genetic patterns that traditional medicine misses.
The Celiac Disease Foundation just launched a $15 million fund to speed up breakthrough solutions for a condition affecting three million Americans, most of whom don't even know they have it. This investment could finally close the gap between patients and the life-changing answers they need.
A new AI system from Shanghai is helping doctors diagnose rare diseases faster and more accurately, even without expensive genetic tests. DeepRare shows its reasoning step by step, making it easier for physicians to trust and verify its conclusions.
Morocco just launched a Precision Medicine Hub that will help thousands of patients with rare diseases get faster diagnoses and coordinated care. The new national center brings together advanced genetic testing, specialist teams, and patient support under one roof.
University of Queensland researchers have developed a breakthrough drug that could transform Motor Neurone Disease from a terminal diagnosis into a manageable chronic condition within five years. The discovery unlocks a previously untargetable immune receptor that plays a key role in neurodegenerative diseases.
Doctors once thought blood tests for Alzheimer's were impossible, but breakthrough technology is now making diagnosis as simple as a routine blood draw. The tests could transform how millions get diagnosed and treated for the disease.
A new AI-powered company is helping families with ultra-rare diseases develop personalized treatments that big pharma overlooks. Founded by a rare disease patient, Nome has already guided more than 10 genetic medicine programs from diagnosis to clinical trials.
When a confidence coach noticed his sex life suffering, he put his own teachings to work. Jonathan George's proactive approach to Peyronie's disease became a masterclass in self-care.
A Nashville family transformed their annual Kentucky Derby party into a powerful fundraiser after their daughter was diagnosed with an incurable nerve disease. Last year alone, they raised $75,000 for research into Charcot-Marie-Tooth disease.
For the first time ever, children and adults with Alexander disease have a treatment that attacks the root cause of their condition, not just the symptoms. The FDA's approval of zilganersen gives hope to families facing a disease that has always been fatal.
A groundbreaking treatment for Huntington's disease just cleared a major hurdle, bringing hope to 240,000 Americans affected by this devastating condition. The experimental therapy could become the first disease-modifying treatment for a disorder that has had none.
A doctor who survived a rare disease now uses artificial intelligence to find unexpected treatments that help patients like Kaila Mabus, who was told she might not survive. His AI system tests 75 million possible drug-disease combinations in minutes.
A groundbreaking treatment for myotonic dystrophy type 1 reduced toxic proteins by 40% and improved muscle function in patients who've never had disease-modifying options. The New England Journal of Medicine just published results that could lead to the first approved therapy for this progressive, often fatal disease.
Researchers discovered how to disguise healthy mitochondria so they can slip into diseased cells undetected, extending the lives of mice with a fatal genetic disorder. The breakthrough could one day help children born with rare mitochondrial diseases.
A new treatment for a rare kidney disease just passed a major test, bringing hope to 330,000 patients in the U.S. and Europe. Vertex's drug successfully reduced a key disease marker by half in late-stage trials.
NFL Pro Bowler Ahman Green is turning his early-onset Parkinson's diagnosis into advocacy, showing others that an early catch gives hope. The four-time Pro Bowl running back is staying ahead of the disease through healthy living and treatment.
Pearl Jam's Eddie Vedder and Canadian director Matt Finlin created a documentary following the race to cure epidermolysis bullosa, a devastating skin disease affecting children worldwide. The Netflix film captures breakthrough research that could unlock treatments for thousands of rare diseases.
A family's agonizing years-long wait for their child's rare disease diagnosis has sparked an artificial intelligence breakthrough in Boca Raton that could help thousands of other families get answers faster. The innovative system is already showing promise in identifying conditions that typically take years to diagnose.
For the first time, a gene therapy has shown dramatic results in slowing Huntington's disease, offering hope to 8,000 UK families who've had no treatment options until now. Patients receiving the higher dose experienced 75% less disease progression over three years.
When Julia Friar's newborn son was diagnosed with a life-threatening genetic disorder, she transformed her fear into action. Now she's helping families across the country while fundraising for a cure.
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