Rare Disease Symposium 2026

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Where Science Meets Silence: Innovations in Rare Diseases


đź“… February 13, 2026 8:30am-6:00pm PST

📍 William J. Rutter Center (Robertson Auditorium) at UCSF Mission Bay (1675 Owens St, San Francisco, CA 94158)
 

 

 Register Free

 


Program

The Rare Disease Symposium 2026 is hosted by the UCSF Catalyst Program and Institute for Human Genetics, in partnership with Foundation Ipsen. Rare diseases affect more than 350 million people worldwide. With a focus on the interdisciplinary development of new diagnostics, new therapeutics, and social advances for patients and their families affected by a rare disease, we hope all participants come away from this symposium with an expanded understanding of the field and the inspiration to make an impact.


Agenda

Time

Who

Title

Topic

Check-in with Light Breakfast

8:30

Welcome & Opening Remarks

9:00

Roopa Ramamoorthi

Director, Catalyst Program, UCSF

Event logistics overview

Catalyst Program and Innovation Ventures

James Levine

President, Foundation Ipsen

Foundation Ipsen

Opening Fireside Chat (tentative)

9:15

Gini Deshpande

CEO, NuMedii

Atul Butte’s legacy in rare cancer and “scalable privilege”

Guy Kawasaki

Chief Evangelist, Canva

Innovation and experience with living with Meniere’s disease

Rare Disease Genetics Overview

10:00

Nadav Ahituv

Director, Institute for Human Genetics, UCSF

Rare diseases with hearing loss overview (e.g., Stickler, Usher’s; of 7,000 rare diseases, ~400 involve hearing loss)

Morning Panel: Drug Discovery in Rare Diseases

10:30

Fyodor Urnov

Director, CRISPR Cures Center

$20M initiative for pediatric rare diseases

Aaron Tward

Chief Scientific Officer, Akouos

Former UCSF Catalyst awardee

Gene therapy for hearing loss

Dylan Chan

or

Russ Dahl

Professor of Otolaryngology, UCSF

CSO, Jacaranda Biosciences

Luke Gruenert

Director, Strategic Innovation, Chiesi Global Rare Diseases

Photography & Human Perspective in Rare Disease

12:00

Rick Guidotti

Founder and CEO, Positive Exposure

Film Screening:

Angelman in Frame film: Angels on Earth

Lunch

12:30

Afternoon Keynote (tentative)

1:30

James Sabry

Chief Business Officer and EVP, BioMarin

Patient Story (Prelude to Panel)

2:00

Patient speaker TBD

Personal journey with rare disease hearing loss

Afternoon Panel: New Technologies & Diagnosis for Hearing Loss

2:20

Dylan Chan

Professor of Otolaryngology, UCSF; cochlear implants expert

Pediatric hearing loss and genetics of hearing loss

Konstantina Stankovic

Otorhinolaryngologist, Stanford

Cochlear imaging technology

Revolutionary diagnostics currently available

Nancy Young

Otolaryngologist, Lurie Children’s Hospital Chicago/Northwestern

AI powered personalized pediatric care

Closing Patient Keynote

4:00

Rebecca Alexander

Author, Motivational Speaker, Psychotherapist, Mental Health Educator, Disability Rights Advocate, and Fitness Coach

Living with Usher syndrome — hearing and vision loss

Concluding Remarks

4:20

Nadav Ahituv

Director, Institute for Human Genetics, UCSF

Highlighting key take aways

Reception

4:30