Through policy framework shifts, appeals to the court for rare disease funds, and starting a centre in Bengaluru, Prasanna ...

The fatty membrane surrounding every living cell is a vibrant environment where countless biological processes take place.

Alkaptonuria is a rare genetic disorder that causes black urine due to homogentisic acid buildup, leading to joint pain, ...

Three patients with spinal muscular atrophy had improved muscle strength and could walk farther after a month of daily spinal ...

Advocacy groups urge Health Ministry to intervene urgently in delayed funding for rare disease treatments, impacting patients ...

A world-leading study screening up to 100,000 newborn babies in England for more than 200 rare genetic conditions has now ...

The pact is the latest in a string of agreements signed in recent years that will contribute to a significant upsurge in local pharmaceutical manufacturing capacity in Oman ...

While this may seem like a very small number, there are in fact more than 6000 rare diseases that we know of today, 80% of which are of genetic origin, often both chronic and life-threatening.

chu-montpellier.fr In adulthood, spinal cord MRI abnormalities such as T2-weighted hyperintensities and atrophy are commonly associated with a large variety of causes (inflammation, infections, ...

A new National Genomic Test Directory for Rare and Inherited Disease (Test Directory) has been launched. The development and ...

AI-driven genomics startups leverage technology to analyze genetic data, predict predispositions, and offer personalized ...

Set to enter hospice care, a patient with idiopathic multicentric Castleman's disease is now in remission after treatment with a medication identified by an AI-guided analysis.