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Proc Natl Acad Sci U S A ; 115(24): E5516-E5525, 2018 06 12.
Artigo em Inglês | MEDLINE | ID: mdl-29844171

RESUMO

De novo variants in SCN2A developmental and epileptic encephalopathy (DEE) show distinctive genotype-phenotype correlations. The two most recurrent SCN2A variants in DEE, R1882Q and R853Q, are associated with different ages and seizure types at onset. R1882Q presents on day 1 of life with focal seizures, while infantile spasms is the dominant seizure type seen in R853Q cases, presenting at a median age of 8 months. Voltage clamp, which characterizes the functional properties of ion channels, predicted gain-of-function for R1882Q and loss-of-function for R853Q. Dynamic action potential clamp, that we implement here as a method for modeling neurophysiological consequences of a given epilepsy variant, predicted that the R1882Q variant would cause a dramatic increase in firing, whereas the R853Q variant would cause a marked reduction in action potential firing. Dynamic clamp was also able to functionally separate the L1563V variant, seen in benign familial neonatal-infantile seizures from R1882Q, seen in DEE, suggesting a diagnostic potential for this type of analysis. Overall, the study shows a strong correlation between clinical phenotype, SCN2A genotype, and functional modeling. Dynamic clamp is well positioned to impact our understanding of pathomechanisms and for development of disease mechanism-targeted therapies in genetic epilepsy.


Assuntos
Potenciais de Ação/genética , Epilepsia/genética , Canal de Sódio Disparado por Voltagem NAV1.2/genética , Adolescente , Adulto , Encefalopatias/genética , Criança , Pré-Escolar , Feminino , Estudos de Associação Genética/métodos , Variação Genética/genética , Genótipo , Humanos , Lactente , Recém-Nascido , Masculino , Fenótipo , Convulsões/genética , Espasmos Infantis/genética , Adulto Jovem
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