Rare disease news, mapped to the diseases behind the headlines. AI-classified across pipeline, policy, funding, science, and community.
Be among the first to receive Kisho Intelligence Briefings
Showing news related to
Showing 1–2 of 2 stories
A study investigates the use of oxytocin in infants with Prader-Willi syndrome to enhance dysphagia and overall disease trajectory. This research could provide insights into new therapeutic approaches for managing symptoms associated with this rare genetic disorder.
Rare Disease Day 2026 aims to raise awareness for over 300 million people living with rare diseases, including Prader-Willi Syndrome. The event highlights the advocacy efforts of individuals like Dr. McTighe, who has dedicated her research and training to support those affected by this condition.
Get the week's most important rare disease developments — pipeline moves, policy changes, and funding signals — delivered to your inbox every Monday.
Free weekly briefing. Unsubscribe anytime.