Hereditary Hemorrhagic Telangiectasia Panel

This product is only meant for customers who already purchased a Dante Genome Test

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.
This panel 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.

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • 6 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Telangiectasia, hereditary hemorrhagic, type 2
  • Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome
  • Capillary malformation-arteriovenous malformation 1

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