| Literature DB >> 23483447 |
Gerhard Kluger1, Udo Koehler, Teresa M Neuhann, Tom Pieper, Martin Staudt, Celina von Stülpnagel.
Abstract
BACKGROUND: There are only few reports on patients with duplications of the short arm of chromosome 5, with little information about concomitant epilepsy. PATIENTS: We report on two patients with generalized epilepsies since age 2.5 years, in whom array comparative genomic hybridization revealed microduplications of different sizes in the short arm of chromosome 5. Both patients showed developmental delay, and magnetic resonance images were normal. The larger duplication in patient 1, who additionally exhibited dysmorphic features and photosensivity on electroencephalogram, occurred de novo, whereas the smaller duplication in patient 2 was paternally inherited. DISCUSSION: The overlapping duplicated region in band 5p13.1 comprises four genes (RICTOR, FYB, C9, and DAB2). Further investigation on patients with duplication 5p and epilepsy are needed to possibly identify a potential susceptibility locus for epilepsy at chromosome 5p13.1. Georg Thieme Verlag KG Stuttgart · New York.Entities:
Mesh:
Year: 2013 PMID: 23483447 DOI: 10.1055/s-0033-1333872
Source DB: PubMed Journal: Neuropediatrics ISSN: 0174-304X Impact factor: 1.947