Hereditary Hemorrhagic Telangiectasia Report
Hereditary Hemorrhagic Telangiectasia
Hereditary Hemorrhagic Telangiectasia is an anomaly of vascular development, characterized by the absence of capillaries normally present between arteries and veins. As a consequence, the spaces between these blood vessels, filled with fragile connections, become responsible for spontaneous severe bleeding such as nosebleeds, strokes, bleeding in the digestive tract and anemia. HHT is a genetic disorder in which a positive family history represents a strong risk factor.
6 genes analyzed genes analyzed
It is recommended if:
This report is useful for those with a positive family history of the condition and/or who experience spontaneous bleeding, even severe, without any other proven cause.
List of main conditions:
- Telangiectasia, hereditary hemorrhagic, type 2
- Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome
- Capillary malformation-arteriovenous malformation 1
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