Correlation Engine 2.0
Clear Search sequence regions

Sizes of these terms reflect their relevance to your search.

Channelopathies are disorders caused by abnormal ion channel function in differentiated excitable tissues. We discovered a unique neurodevelopmental channelopathy resulting from pathogenic variants in SCN3A, a gene encoding the voltage-gated sodium channel NaV1.3. Pathogenic NaV1.3 channels showed altered biophysical properties including increased persistent current. Remarkably, affected individuals showed disrupted folding (polymicrogyria) of the perisylvian cortex of the brain but did not typically exhibit epilepsy; they presented with prominent speech and oral motor dysfunction, implicating SCN3A in prenatal development of human cortical language areas. The development of this disorder parallels SCN3A expression, which we observed to be highest early in fetal cortical development in progenitor cells of the outer subventricular zone and cortical plate neurons and decreased postnatally, when SCN1A (NaV1.1) expression increased. Disrupted cerebral cortical folding and neuronal migration were recapitulated in ferrets expressing the mutant channel, underscoring the unexpected role of SCN3A in progenitor cells and migrating neurons. Copyright © 2018 Elsevier Inc. All rights reserved.


Richard S Smith, Connor J Kenny, Vijay Ganesh, Ahram Jang, Rebeca Borges-Monroy, Jennifer N Partlow, R Sean Hill, Taehwan Shin, Allen Y Chen, Ryan N Doan, Anna-Kaisa Anttonen, Jaakko Ignatius, Livija Medne, Carsten G Bönnemann, Jonathan L Hecht, Oili Salonen, A James Barkovich, Annapurna Poduri, Martina Wilke, Marie Claire Y de Wit, Grazia M S Mancini, Laszlo Sztriha, Kiho Im, Dina Amrom, Eva Andermann, Ritva Paetau, Anna-Elina Lehesjoki, Christopher A Walsh, Maria K Lehtinen. Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development. Neuron. 2018 Sep 05;99(5):905-913.e7

Expand section icon Mesh Tags

Expand section icon Substances

PMID: 30146301

View Full Text