Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6012304 | Epilepsy & Behavior | 2014 | 4 Pages |
Abstract
Lennox-Gastaut syndrome (LGS) is an epileptic encephalopathy with a heterogeneous etiology. In this study, we aimed to explore the role of CHD2 in LGS, as CHD2 mutations have been described recently in various epileptic encephalopathies. We have previously identified one patient with a large deletion affecting the CHD2 gene in a group of 22 patients with LGS or LGS-like epilepsy. In the remaining 17 patients without known etiology, Sanger sequencing revealed a de novo 1-bp duplication in the CHD2 gene in another patient. This mutation leads to a frameshift and, consequently, a premature stop codon 49Â bp downstream of the mutation. The patient had prominent myoclonic seizures and photosensitivity, thus, sharing phenotypic features with previously reported patients with CHD2-related epilepsy. In our original material of 22 patients with LGS features, we have now found two (9%) with mutations in the CHD2 gene. Our findings suggest that CHD2 mutations are important in the etiological spectrum of LGS.
Related Topics
Life Sciences
Neuroscience
Behavioral Neuroscience
Authors
Caroline Lund, Eylert Brodtkorb, Ane-Marte Ãye, Oddveig Røsby, Kaja Kristine Selmer,