Please use this identifier to cite or link to this item:
Title: Evidence of linkage to chromosome 5p13.2-q11.1 in a large inbred family with genetic generalized epilepsy.
Austin Authors: Kinay, Demet;Oliver, Karen L;Tüzün, Erdem;Damiano, John A;Ulusoy, Canan;Andermann, Eva;Hildebrand, Michael S ;Bahlo, Melanie;Berkovic, Samuel F 
Affiliation: Okmeydani Education and Research Hospital, Istanbul, Turkey..
Epilepsy Research Centre, Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia
Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia
Department of Neuroscience, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey
Neurogenetics Unit, Montreal Neurological Hospital and Institute, Montreal, Quebec, Canada
Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia
Issue Date: Aug-2018
Date: 2018-07-04
Publication information: Epilepsia 2018; 59(8): e125-e129
Abstract: The clinical genetics of genetic generalized epilepsy suggests complex inheritance; large pedigrees, with multiple affected individuals, are rare exceptions. We studied a large consanguineous family from Turkey where extensive electroclinical phenotyping revealed a familial phenotype most closely resembling juvenile myoclonic epilepsy. For a subject to be considered affected (n = 14), a diagnostic electroencephalogram was required. Seizure onset ranged between 6 and 19 years (mean = 12 years). Thirteen of 14 experienced myoclonic jerks; in 11, this was associated with eyelid blinking, and in 10 it was interspersed with absences. Generalized tonic-clonic seizures were seen in 11. One individual had generalized tonic-clonic seizures alone. Electroencephalograms demonstrated generalized polyspike and wave discharges that were not associated with photoparoxysmal response. Intellect was normal. Nineteen family members were subsequently chosen for nonparametric multipoint linkage analyses, which identified a 39.5 Mb region on chromosome 5 (P < 0.0001). Iterative analysis, including discovery of a subtly affected individual, narrowed the critical region to 15.4 Mb and possibly to 5.5 Mb. Homozygous versus heterozygous state of the refined 5p13.2-q11.1 haplotype was not associated with phenotypic severity or onset age, suggesting that one versus two pathogenic variants may result in similar phenotypes. Whole exome sequencing (n = 3) failed to detect any rare, protein-coding variants within the highly significant linkage region that includes HCN1 as a promising candidate.
DOI: 10.1111/epi.14506
ORCID: 0000-0003-4580-841X
Journal: Epilepsia
PubMed URL: 29974457
Type: Journal Article
Subjects: HCN1
juvenile myoclonic epilepsy
linkage analysis
Appears in Collections:Journal articles

Show full item record

Page view(s)

checked on Sep 29, 2023

Google ScholarTM


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.