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Test Code 10131

Hereditary Hemorrhagic Telangiectasia (HHT) Panel

6 genes

2 - 3 weeks (7 - 16 days STAT)

Who is this test for?
  • Individuals with relevant features who have a clinical or suspected diagnosis of HHT or Capillary Malformation-Arteriovenous Malformation (CM-AVM) syndrome 
  • Individuals with capillary malformations, “port wine stains”, arteriovenous malformations, frequent nosebleeds, mucosal telangiectases, or any degree of GI, pulmonary, or cerebral hemorrhage 
  • Individuals with negative results from previous single-gene HHT testing 
  • Individuals who have a family history of HHT
Method
NGS with CNV (Exome or Genome Platform)
Specimen(s)

Exome Platform: Blood, DNA, Buccal, Saliva, Tissue

Genome Platform: Blood, DNA

Order Options

Platform
Test type
OTHER OPTIONS
for pricing.

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