Abstract
The interplay of multiple genetic factors, as opposed to monogenic inheritance, is suspected to play a role in many idiopathic generalized epilepsies. This leads to a digenic or oligogenic inheritance model, which although rather simplified, may explain at least some of the clinical observations. Here we describe a family in which the clinical phenotype in the offspring can be explained by a combination of photosensitivity and epilepsy traits that segregated independently of each other. This case history demonstrates the need to evaluate family histories in more detail in order to uncover potential clinical markers for genetic factors in complex epilepsies.
Original language | English |
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Pages (from-to) | 32-36 |
Number of pages | 5 |
Journal | Epileptic Disorders |
Volume | 8 |
Issue number | 1 |
State | Published - Mar 2006 |
Externally published | Yes |
Keywords
- Biparental inheritance
- Genetics
- Juvenile myoclonic epilepsy
- Oligogenic
- Photosensitive epilepsy