Hereditary Hemorrhagic Telangiectasia (HHT)
HHT is a genetic condition that causes enlargements and tangles of veins and arteries (telangiectasias) and other malformations of the blood vessels. These can occur in the brain, lungs, digestive system, skin or other organs. HHT is somewhat rare, affecting approximately 1 in 5,000 people. It does not occur more frequently among people of any gender or racial or ethnic background. The main symptoms of hereditary hemorrhagic telangiectasia involve blood vessel malformations that can cause bleeding. Telangiectasias and other AVMs in people with HHT can form from birth until adulthood, and may occur in several organs of the body.
- Patient Support and Education
- Care Coordination
- Advocacy Efforts
Related Conference of Hereditary Hemorrhagic Telangiectasia (HHT)
March 23-24, 2026
13th International Conference on Hypertension and Cardiovascular Diseases
London, UK
May 21-22, 2026
13th World Congress on Hypertension, Cardiology, Primary Health and Patient Care
Paris, France
July 23-24, 2026
13th International Conference on Geriatric Cardiology, Cardiovascular Diseases and Palliative Care
Paris, France
Hereditary Hemorrhagic Telangiectasia (HHT) Conference Speakers
Recommended Sessions
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- Emerging Biomarkers in Cardiovascular Disease
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- Hereditary Hemorrhagic Telangiectasia (HHT)
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