Items related to SCN2A Related Disorders (Elements in Genetics in Epilepsy)
Synopsis
Reviews clinical, genetic and pathophysiological features and treatment of neurodevelopmental disorders caused by variants in the voltage-gated sodium channel gene, SCN2A.
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SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
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Cambridge University Press, 2025
ISBN 10: 1009530372
ISBN 13: 9781009530378
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Scn2a-related Disorders
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ISBN 10: 1009530372
ISBN 13: 9781009530378
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SCN2A-Related Disorders (Paperback or Softback)
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SCN2A Related Disorders (Elements in Genetics in Epilepsy)
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Cambridge University Press, 2025
ISBN 10: 1009530372
ISBN 13: 9781009530378
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SCN2A-Related Disorders
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Paperback. Condition: New. SCN2A encodes a voltage-gated sodium channel (designated NaV1.2) vital for generating neuronal action potentials. Pathogenic SCN2A variants are associated with a diverse array of neurodevelopmental disorders featuring neonatal or infantile onset epilepsy, developmental delay, autism, intellectual disability and movement disorders. SCN2A is a high confidence risk gene for autism spectrum disorder and a commonly discovered cause of neonatal onset epilepsy. This remarkable clinical heterogeneity is mirrored by extensive allelic heterogeneity and complex genotype-phenotype relationships partially explained by divergent functional consequences of pathogenic variants. Emerging therapeutic strategies targeted to specific patterns of NaV1.2 dysfunction offer hope to improving the lives of individuals affected by SCN2A-related disorders. This Element provides a review of the clinical features, genetic basis, pathophysiology, pharmacology and treatment of these genetic conditions authored by leading experts in the field and accompanied by perspectives shared by affected families. This title is also available as Open Access on Cambridge Core. Seller Inventory # LU-9781009530378
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Scn2a-related Disorders
Published by
Cambridge University Press, 2025
ISBN 10: 1009530372
ISBN 13: 9781009530378
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SCN2A-Related Disorders (Paperback)
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ISBN 10: 1009530372
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Paperback. Condition: new. Paperback. SCN2A encodes a voltage-gated sodium channel (designated NaV1.2) vital for generating neuronal action potentials. Pathogenic SCN2A variants are associated with a diverse array of neurodevelopmental disorders featuring neonatal or infantile onset epilepsy, developmental delay, autism, intellectual disability and movement disorders. SCN2A is a high confidence risk gene for autism spectrum disorder and a commonly discovered cause of neonatal onset epilepsy. This remarkable clinical heterogeneity is mirrored by extensive allelic heterogeneity and complex genotype-phenotype relationships partially explained by divergent functional consequences of pathogenic variants. Emerging therapeutic strategies targeted to specific patterns of NaV1.2 dysfunction offer hope to improving the lives of individuals affected by SCN2A-related disorders. This Element provides a review of the clinical features, genetic basis, pathophysiology, pharmacology and treatment of these genetic conditions authored by leading experts in the field and accompanied by perspectives shared by affected families. This title is also available as Open Access on Cambridge Core. This Element provides a review of the clinical features, genetic basis, pathophysiology, pharmacology and treatment of these genetic conditions authored by leading experts in the field and accompanied by perspectives shared by affected families. This title is also available as Open Access on Cambridge Core. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. Seller Inventory # 9781009530378
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SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
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Cambridge University Press, 2025
ISBN 10: 1009530372
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SCN2A-Related Disorders (Elements in Genetics in Epilepsy)
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SCN2A Related Disorders (Elements in Genetics in Epilepsy)
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