TGen's Center for Rare Childhood Disorders, C4RCD, is giving hope to children and their families where once there was none.

After years following diagnostic odysseys across the nation, and even other countries, TGen's advanced genomic research is providing answers and hope to hundreds of children. After arriving at TGen, often with just a collection of symptoms, our diagnoses help put physicians on the right track towards treating the most vulnerable among us.

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Faculty

Matt Huentelman

Matt Huentelman Ph.D.

Professor
Neurogenomics Division

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Vinodh Narayanan

Vinodh Narayanan M.D.

Clinical Professor and Medical Director
Center for Rare Childhood Disorders

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Sampathkumar Rangasamy

Sampathkumar Rangasamy Ph.D.

Research Assistant Professor
Neurogenomics

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Rare Childhood Disorders

We conduct genomic sequencing to end the diagnostic odyssey for rare disease patients and their families.

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