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Average age of onset is approximately 12 years but ranges from infancy to adulthood. Although nosebleeds are often spontaneous, they also occur more often in patients with HHT secondary to minimal trauma to the nose.
The most common symptom of HHT by far is nosebleeds, affecting about 90 percent of people with HHT. These can happen daily and often first occur in childhood. Those with abnormal GI tract blood vessels should watch for dark stools or blood in the stool.
HHT is a genetic condition that causes s 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.
The researchers also found slight variations in life expectancy ing to HHT type. People with type 1 HHT, which is caused by a mutation in the ENG gene, had an average life expectancy of 76.4 years. People with type 2 HHT, which involves a mutation in the ACVRL1 gene, had a life expectancy of 77.9 years.
HHT is a genetic disorder in which blood vessels do not develop normally leading to bleeding that can be serious or life threatening. Frequent nosebleeds are the most common sign.
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HHT is a genetic disorder of the blood vessels that affects people of all ages and backgrounds. An estimated 50,000 to 100,000 Americans are affected by HHT, and most cases go undiagnosed. About 10 percent of people with HHT die prematurely or are disabled due to complications of their AVMs.
The most common symptom is frequent nosebleeds (epistaxis). Some people with HHT also might have delicate red spots on certain parts of the body. They may get lighter when you press on them and are common on the: Face.
Nosebleeds are often the first sign of HHT. They may be frequent and persistent. They happen because of the abnormal blood vessels in the lining of the nose. The loss of blood can lead to iron-deficiency anaemia, if the iron is not replaced through the diet and with iron supplements.

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