Baby born with cloudy eyes is one of just 23 in world with rare genetic disease
The mum and dad of a baby with a genetic disease so rare it has no name have vowed to keep fighting for him after the ...
News Medical on MSN4h
AI approach reveals possible fusion of rare diseases in COVID-19 origins In A Landmark Dis...
Despite extensive research, the origins of COVID-19 remain elusive. In a new study published in the KeAi journal Advances in Biomarker Sciences and Technology (ABST), an AI-driven approach was adopted ...
EurekAlert!1d
Uncovering two rare infectious diseases which might be responsible for COVID-19
In a landmark discovery, researchers applied a novel AI model called the max-logistic intelligence classifier to analyze ...
'Doctors say our baby won't live two months after they saw rare sign'
A baby is one of just 23 in the world diagnosed with a rare genetic disease - after doctors spotted his eyes were cloudy at ...
Texas Public Radio4d
Spinal stimulation restored muscles wasted by rare genetic disorder
Three patients with spinal muscular atrophy had improved muscle strength and could walk farther after a month of daily spinal ...
Gene therapy and bone marrow transplant alleviate ultra-rare genetic disease symptoms
In two new papers, researchers from The Jackson Laboratory (JAX) report the successful use of two approaches—gene therapy and ...
Ozzy Osbourne's ‘rare’ genetic diagnosis leaves him battling 'more than 40 symptoms'
Ozzy Osbourne revealed he had been hiding a secret from his fans. He had been diagnosed with Parkinson’s Disease the year ...
Rare disease patients and advocacy groups appeal to PM Modi for sustainable funding for treatment
Families of rare disease patients appeal to PM Modi and Health Minister for increased treatment funding support.
BioTechniques11d
Long-read sequencing expedites rare disease diagnoses
Long-read sequencing is being harnessed to improve the rate of rare disease diagnosis. Researchers at the University of California Santa Cruz (CA, USA) have demonstrated that long-read sequencing (LRS ...
TheBetterIndia4d
‘No One Should Face This’: After Losing Daughter, Dad Ensures No Rare Disease Patient Suffers Alone
Through policy framework shifts, appeals to the court for rare disease funds, and starting a centre in Bengaluru, Prasanna ...
India Today12d
Rare disease patients in crisis as delays stall national policy implementation
Patient advocacy groups warned that delays in implementing India's rare disease policy have left many, including children, in ...
Delay in roll out of ₹974 crore under rare diseases policy hits patients
Advocacy groups urge Health Ministry to intervene urgently in delayed funding for rare disease treatments, impacting patients ...