Abstract
It has been suggested [3, 6] that juvenile myoclonic epilepsy (JME) may follow a polygenic threshold pattern of inheritance — specifically, with a differential sex effect, in that females are more often affected than males. However, as described below, we have examined 78 families with JME from Berlin and 27 from Los Angeles and have found no evidence to support the polygenic hypothesis for pure JME, either with or without differential thresholds for the two sexes. We could reach no conclusion when we included other epilepsies or EEG abnormalities in our definition of the trait.
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References
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© 1989 Springer-Verlag Berlin Heidelberg
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Hodge, S.E., Greenberg, D.A., Durner, M., Delgado-Escueta, A.V., Janz, D. (1989). Is Juvenile Myoclonic Epilepsy Polygenic?. In: Beck-Mannagetta, G., Anderson, V.E., Doose, H., Janz, D. (eds) Genetics of the Epilepsies. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-95553-2_9
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DOI: https://doi.org/10.1007/978-3-642-95553-2_9
Publisher Name: Springer, Berlin, Heidelberg
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