Skip to content

GenTAC Alliance

  • About Us
    • About the Alliance
    • Executive Committee and Working Groups
    • News & Announcements
  • Condition Insights
    • The Aorta & Aortic Dissections
    • Conditions
      • Bicuspid Aortic Valve (BAV)
      • Loeys-Dietz Syndrome
      • Marfan Syndrome
      • Nonsyndromic Heritable Thoracic Aortic Disease (nsHTAD)
      • Turner Syndrome
      • Vascular Ehlers-Danlos Syndrome
    • Genetic Testing for Hereditable Thoracic Aortic Disease
    • Glossary
    • Patient Stories
    • Ask a Question
  • Best Practices & Guidelines
    • Best Practices & Guidelines
    • Clinical Management Videos & Tools
  • Education
    • Continuing Education & Other Courses
    • Webinars
  • Research
    • Registries
    • Publications
    • Funding Opportunities
    • Research Opportunities for Your Patients
  • Webinars
  • Stay Informed
  • Donate
  • Stay Informed
  • Donate

About Us

← Back
  • About the Alliance
  • Executive Committee & Working Groups
  • News & Announcements

Condition Insights

← Back
  • The Aorta and Aortic Dissections
  • Conditions
  • Bicuspid Aortic Valve (BAV)
  • Loeys-Dietz Syndrome (LDS)
  • Marfan Syndrome
  • Nonsyndromic Heritable Thoracic Aortic Disease (nsHTAD)
  • Turner Syndrome
  • Vascular Ehlers-Danlos Syndrome (VEDS)
  • Genetic Testing for Hereditable Thoracic Aortic Disease
  • Glossary
  • Patient Stories
  • Ask a Question

Best Practices & Guidelines

← Back
  • Best Practices & Guidelines
  • Clinical Management Videos & Tools

Education

← Back
  • Continuing Education & Other Courses
  • Webinars

Research

← Back
  • Registries
  • Publications
  • Funding Opportunities
  • Research Opportunities for Your Patients

Webinars

← Back
  • Upcoming & Past Webinars

Home ▶ ▶

Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections.

Share

  • Facebook
  • Twitter
  • Pinterest
  • Email

Related Content

News

Dr. Alan Braverman Discusses Important Role Radiologists Play in Early Marfan Diagnosis

February 13, 2025February 13, 2025

Dr. Alan Braverman, director of the Marfan Syndrome and Aortopathy Center at the Washington...

Read More
Resources

UTHealth Genomic Medicine Guidance App

February 25, 2023October 10, 2023

The UTHealth Genomic Medicine Guidance app is designed for use as a point-of-care...

Read More
Resources

International E3 Summit Presentations Now Available on YouTube

January 4, 2021October 11, 2023

The Marfan Foundation has made the 60 English presentations given during its International...

Read More
  • Stay Informed
  • Search
  • Contact
  • Twitter

The GenTAC Alliance is a division of The Marfan Foundation | Privacy Policy