Comprehensive inherited neuropathy panel

Diagnosis, simplified

Our comprehensive inherited neuropathy panel simplifies the diagnostic process by using next-generation sequencing to evaluate 186 genes with associations to inherited neuropathy. Comprised only of clinically relevant genes, our panel was carefully vetted by a multidisciplinary team of neurologists and geneticists and includes 60 unique genes that enable an enhanced diagnostic yield over traditional testing approaches.

60 unique genes included in our hereditary neuropathy panel

30 genes in our hereditary neuropathy panel have complementary functional testing

10%

10% of cases identified based on evaluation of additional 60 genes¹

Comprehensive inherited neuropathy panel Test menu

Comprehensive inherited neuropathy panel

Key testing

PEPAN | Comprehensive Peripheral Neuropathy Gene Panel, Varies
- Establishes a molecular diagnosis for patients with peripheral neuropathy.
- Offers improved sensitivity of more than 99.9% for both small mutations and copy number variants on all genes and 94.7% on insertions/deletions.
- Identifies variants within genes known to be associated with peripheral neuropathy, allowing for predictive testing of at-risk family members.
- Upon request, this test reflexes to Panel to Whole Exome Sequencing Reflex Test, Varies (Mayo ID: WESPR).

References

Internal Mayo Clinic data.

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