IMPROVING THE LIVES OF THOSE

AFFECTED BY TANGO2 DEFICIENCY DISORDER

OUR

MISSION

The TANGO2 Research Foundation’s mission is to lead the way in finding a cure for TANGO2 deficiency disorder.

OUR

VISION

Accelerate

research and therapy discovery

Advocate

and promote awareness

Support

and connect families

Drive

accurate and early diagnosis

OUR

COMMUNITY

RECENT

NEWS

Spotlight
March 31, 2026

Hero Highlight: Dr. Kuntal Sen

We’re excited to spotlight this month’s Hero Highlight, Dr. Kuntal Sen! Dr. Sen is the Director of the Mitochondrial Disorders Program and Co-Director of the Neurogenetics Clinic at Children’s National Hospital.…
Destiny Braden
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Uncategorized
March 12, 2026

TANGO2 Leaders Share Insights at Rare Disease Symposium

On February 27th, Foundation co-founder, Kasha Morris, Research Director, Deena Chisholm, and TANGO2 parent, Veronica Jones Swetek attended and presented at the Rady Children’s Health Orange County & UC Irvine…
Destiny Braden
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Uncategorized
February 13, 2026

The TANGO2 Research Foundation 2025 Annual Report Is Here

We are proud to share the TANGO2 Research Foundation’s 2025 Annual Report—a reflection of a year defined by growth, progress, and meaningful impact. This report represents more than a summary…
Destiny Braden
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of those living with TANGO2-related deficiency disorder.

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