Difference between revisions of "Genetic screening for SUDEP? – Commentary on Hindocha et al."
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(Created page with "''Tomson T (2008) Genetic screening for SUDEP? – Commentary on Hindocha et al.. Epilepsia 49:2 368–9.'' '''[http://onlinelibrary.wiley.com/doi/10.1111/j.1528-1167.2007.01...") |
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| + | Tomson T (2008) Genetic screening for SUDEP? – Commentary on Hindocha et al.. Epilepsia 49:2 368–9. | ||
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'''First Paragraph:''' In this issue, Neeta Hindocha and colleagues presentan interesting observation of two cases of sudden unexpected death in epilepsy (SUDEP) in a family with GEFS+with a novel SCN1A mutation. It remains to be elucidatedwhether there is a specific association between this mutation and an increased risk of SUDEP, if this is a chancefinding, or if the observations merely reflect the risks associated with refractory epilepsy in general. A SUDEPincidence of 4–7/1,000 person-years, as in this family, iscomparable to rates reported among refractory epilepsypopulations (Tomson et al., 2005). | '''First Paragraph:''' In this issue, Neeta Hindocha and colleagues presentan interesting observation of two cases of sudden unexpected death in epilepsy (SUDEP) in a family with GEFS+with a novel SCN1A mutation. It remains to be elucidatedwhether there is a specific association between this mutation and an increased risk of SUDEP, if this is a chancefinding, or if the observations merely reflect the risks associated with refractory epilepsy in general. A SUDEPincidence of 4–7/1,000 person-years, as in this family, iscomparable to rates reported among refractory epilepsypopulations (Tomson et al., 2005). | ||
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*Brief commentary on Hindocha et al. (2008) | *Brief commentary on Hindocha et al. (2008) | ||
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Latest revision as of 13:32, 17 June 2019
Tomson T (2008) Genetic screening for SUDEP? – Commentary on Hindocha et al.. Epilepsia 49:2 368–9.
Abstract: First Paragraph: In this issue, Neeta Hindocha and colleagues presentan interesting observation of two cases of sudden unexpected death in epilepsy (SUDEP) in a family with GEFS+with a novel SCN1A mutation. It remains to be elucidatedwhether there is a specific association between this mutation and an increased risk of SUDEP, if this is a chancefinding, or if the observations merely reflect the risks associated with refractory epilepsy in general. A SUDEPincidence of 4–7/1,000 person-years, as in this family, iscomparable to rates reported among refractory epilepsypopulations (Tomson et al., 2005).
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Context
- Brief commentary on Hindocha et al. (2008)
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