Literature DB >> 23483447

Generalized epilepsy in two patients with 5p duplication.

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.

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Year:  2013        PMID: 23483447     DOI: 10.1055/s-0033-1333872

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  2 in total

1.  Novel rearrangements between different chromosomes with direct impact on the diagnosis of 5p- syndrome.

Authors:  Samar Nasser Chehimi; Vanessa Tavares Almeida; Amom Mendes Nascimento; Évelin Aline Zanardo; Yanca Gasparini de Oliveira; Gleyson Francisco da Silva Carvalho; Beatriz Martins Wolff; Marilia Moreira Montenegro; Nilson Antônio de Assunção; Chong Ae Kim; Leslie Domenici Kulikowski
Journal:  Clinics (Sao Paulo)       Date:  2022-05-28       Impact factor: 2.898

Review 2.  Stüve-Wiedemann syndrome: LIFR and associated cytokines in clinical course and etiology.

Authors:  Dawn Mikelonis; Cheryl L Jorcyk; Ken Tawara; Julia Thom Oxford
Journal:  Orphanet J Rare Dis       Date:  2014-03-12       Impact factor: 4.123

  2 in total

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