Mayo Clinic Laboratories > Neurology > Neurogenetics > Hereditary peripheral neuropathy > Comprehensive inherited neuropathy panel

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

60 unique genes included in our hereditary neuropathy panel

30

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 Comprehensive inherited neuropathy panel

Comprehensive inherited neuropathy panel

Key testing

Advantages

  • 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.
References
  1. Internal Mayo Clinic data.
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