Prevention Genetics Logo
Test Code 1329

Hereditary Paraganglioma and Pheochromocytoma Panel

12 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 hereditary paraganglioma/pheochromocytoma
  • Individuals with multiple, multifocal, bilateral, early-onset (<45 years), or familial paragangliomas/pheochromocytomas
  • Individuals with extra-adrenal or metastatic paragangliomas/pheochromocytomas
  • Individuals with SDHB-deficient paragangliomas/pheochromocytomas by immunohistochemistry 
  • Individuals with a personal or family history consistent with a syndromic paraganglioma/pheochromocytoma presentation (MEN1, MEN2, NF1, VHL, HLRCC)
Method
Sequencing with CNV PG-Select
Specimen(s)

Blood, Buccal, Saliva, Tissue

Order Options

Test type
OTHER OPTIONS
for pricing.

Explore related tests

Questions? We can help.

Getting support has never been easier. Connect with our team for assistance with anything from test selection to interpreting results. Use the live chat button or visit our Contact us page.