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Hereditary Hemorrhagic Telangiectasia (HHT) Center

 

Hereditary Hemorrhagic Telangiectasia (HHT)

HHT is an inherited disorder that affects blood vessels. It is characterized by abnormal connections between arteries and veins known as arteriovenous malformations (AVM’s) and telangiectases. AVM’s occur in the brain, spine, liver and lungs. Telangiectases are found in the mucocutaneous surface areas of the gastrointestinal tract, skin and nose.

HHT affects about one in 5,000 people in the United States, though about 90 percent of those who have it are undiagnosed.

Manifestations of HHT include:

  • Recurrent epistaxis (nosebleeds)
  • Telangiectases
  • AVM’s in solid organs

For more information or to schedule an appointment, call 314.454.5437 or 800.678.5437 or email us.

 


 

Hereditary Hemorrhagic Telangiectasia (HHT) Center

 

HHT Team

The HHT Team was  featured in the Washington University School of Medicine Outlook Magazine.  Read more...