Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/55026
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Type: Journal article
Title: Clinical Study of Two Brothers With a Novel 33 bp Duplication in the ARX Gene
Author: Demos, M.
Fullston, T.
Partington, M.
Gecz, J.
Gibson, W.
Citation: American Journal of Medical Genetics. Part A, 2009; 149A(7):1482-1486
Publisher: Wiley-Liss
Issue Date: 2009
ISSN: 1552-4825
1552-4833
Statement of
Responsibility: 
Michelle K. Demos, Tod Fullston, Michael W. Partington, Jozef Gécz and William T. Gibson
Abstract: Pathogenic variations of the ARX (aristaless-related homeobox) gene are associated with marked phenotypic pleiotropy. These phenotypes are X-linked neurological disorders that include brain and genital malformation and non-malformation syndromes. Typically, malformation phenotypes result from pathogenic variations that are predicted to truncate the ARX protein, or alter residues in the highly conserved homeodomain. While non-malformation phenotypes tend to be caused by pathogenic variations that are predicted to expand the first two polyalanine tracts of ARX, or alter residues outside of the homeodomain. The most common pathogenic variation of the ARX gene is a duplication of 24 bp, c.429_452 dup, which leads to an expansion of the second polyalanine tract of the ARX protein from 12 to 20 alanine residues. This pathogenic variation is associated with both sporadic and familial nonsyndromic mental retardation. Syndromic manifestations include mental retardation with hand dystonia (Partington syndrome), infantile spasms (West syndrome) and/or other epileptic seizures. Here, we report on a novel pathogenic variant of a tandem 33 bp duplication that is predicted to result in an expansion of polyalanine tract 2 in two brothers with mental retardation, epilepsy, dystonia, and the novel feature of intermittent hyperventilation. This pathogenic variation is predicted to result in a "non-homogeneous" polyalanine tract expansion that is longer than predicted expansion caused by the common 24 bp duplication. The location of the novel 33 bp duplication in the same region as the common 24 bp duplication supports this region as the ARX variation "hot spot."
Keywords: ARX gene; polyalanine expansions; dystonia; seizures
RMID: 0020091024
DOI: 10.1002/ajmg.a.32851
Appears in Collections:Paediatrics publications

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