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Article

FDG PET Findings in Rare Brain Sodium Channelopathy Associated with SCN2A Gene Mutation.

Clinical nuclear medicine - 1 Apr 2026

Seniaray Nikhil, Verma Ritu, Kumar Praveen, Belho Ethel

Abstract excerpt

SCN2A gene mutations, which affect the function of the voltage-gated sodium channel NaV1.2, are associated with a spectrum of neurological disorders, including epileptic encephalopathies and autism spectrum disorders. Advanced imaging modalities such as magnetic resonance imaging (MRI) and positron emission tomography (PET) have been instrumental in elucidating the neuroanatomic and functional alterations...

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Brain
Channelopathies
Fluorodeoxyglucose F18
Mutation
NAV1.2 Voltage-Gated Sodium Channel

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Positron-Emission Tomography

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PMID: 40929566
DOI: 10.1097/RLU.0000000000006110

Genes

SCN2A

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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