Welcome to the Trisomy 18 Foundation Patient Insights Network

  

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W
elcome to the Trisomy 18 Patient Insights Network (PIN), a research database of families and children impacted by a Trisomy 18 diagnosis. The purpose of this registry is to accelerate interest and investment in biomedical research to further Trisomy 18 knowledge, and to advance treatments.
 
This PIN is developed with the generous support of friends and families in the Trisomy 18 Foundation. To learn more about Trisomy 18 and how to support the development of the registry, please visit www.trisomy18.org.
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W
elcome to the Trisomy 18 Patient Insights Network (PIN), a research database of families and children impacted by a Trisomy 18 diagnosis. The purpose of this registry is to accelerate interest and investment in biomedical research to further Trisomy 18 knowledge, and to advance treatments.
 
This PIN is developed with the generous support of friends and families in the Trisomy 18 Foundation. To learn more about Trisomy 18 and how to support the development of the registry, please visit www.trisomy18.org.

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