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Alagille Syndrome: Genetically Speaking

Featuring Dr. David Piccoli and Dr. Nancy Spinner

The ALGSA’s first video documentary film features Dr. David Piccoli and Dr. Nancy Spinner, as they recount their involvement in the discoveries of the Jagged 1 and Notch 2 genes associated with Alagille Syndrome, both paramount milestones in the progression of understanding ALGS through the decades. A witty and entertaining short film, Dr. Piccoli and Dr. Spinner take us step by step and acknowledge many of the brilliant minds who participated.

An Alagille Syndrome Alliance Film | A Cincore Media Production

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Alagille Syndrome: Genetically Speaking

Featuring Dr. David Piccoli and Dr. Nancy Spinner

The ALGSA’s first video documentary film features Dr. David Piccoli and Dr. Nancy Spinner, as they recount their involvement in the discoveries of the Jagged 1 and Notch 2 genes associated with Alagille Syndrome, both paramount milestones in the progression of understanding ALGS through the decades. A witty and entertaining short film, Dr. Piccoli and Dr. Spinner take us step by step and acknowledge many of the brilliant minds who participated.

An Alagille Syndrome Alliance Film | A Cincore Media Production

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Alagille Syndrome Alliance: Founder’s Story

Featuring Cindy Luxhoj, ALGSA Founder

This film takes a look back at how the Alagille Syndrome Alliance was founded and the legacy of Alaina K Hahn, the founder’s daughter who lived with ALGS. Cindy Luxhoj shares her journey with starting the organization, its purpose, and her daughter’s contribution to the cause throughout her life.

An Alagille Syndrome Alliance Film

A Larsen Films Production

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