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Gain-of-function mutation Met136Val in SCN8A may not be a common cause of trigeminal neuralgia
Raymond F Sekula1, Kathleen Deeley2, Hayley Denwood1
1Department of Neurosurgery, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Molecular Genetics & Genomic Medicine
|January 11, 2021
Abstract
Background:
The Met136Val mutation in SCN8A was described in a case of trigeminal neuralgia but no frequency among affected individuals was provided.
Methods:
Direct sequencing of 123 individuals diagnosed with classic trigeminal neuralgia was performed aimed to detect the Met136Val change.
Results:
No cases of classical trigeminal neuralgia studied had the Met136Val mutation in SCN8A.
Conclusion:
Met136Val mutation in SCN8A is not a frequent cause of classical trigeminal neuralgia.

