The scientists and doctors at TGen’s Center for Rare Childhood Disorders use genomic sequencing to pinpoint the causes of rare or unknown disorders that largely go undetected with conventional testing. Their efforts have ended the diagnostic odyssey for a number of children and their families who have undergone countless exams and procedures only to come up empty. With your support we can bring hope — and answers — to many more. Your gift enables TGen's Center for Rare Childhood Disorders to provide hope and answers to rare disease patients.

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Matt Huentelman Ph.D.

Professor and Director
Neurogenomics Division

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Vinodh Narayanan M.D.

Clinical Professor and Medical Director
Center for Rare Childhood Disorders

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Sampathkumar Rangasamy Ph.D.

Research Associate Professor

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Contact Information

Please contact the TGen Foundation at:

Campbell Faulkner

Meet Campbell Faulkner, a 12-year-old with a rare genetic disorder that primarily affects children.

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