PTPN11

Learn more about the PTPN11 gene and connect with other Simons Searchlight families with the resources below:

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Support Resources

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GeneReviews

GeneReviews are a great resource to bring to your child’s clinicians. These publications provide a summary of current research on genetic conditions and information on ongoing care.

Noonan Syndrome is often caused by a gene change in PTPN11 or other Noonan Syndrome genes (GeneReviews linked here).

Check out the GeneReviews for Noonan Syndrome.

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Research Article Summaries

We currently do not have any article summaries for PTPN11, but we add resources to our website as they become available.

The information available about PTPN11 is limited, and families and doctors share a critical need for more information. As we learn more from children who have this gene change, we expect our list of resources and information to grow.

You can also visit the Simons Foundation ’s SFARI Gene website to see information for researchers about this gene.

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Research Opportunities

Simons Searchlight

Help the Simons Searchlight team learn more about PTPN11 genetic changes by taking part in our research. You can learn more about the project and sign up here.

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Family Stories

We do not currently have any stories from PTPN11 families.

Click here to share your family’s story!