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ATRX syndrome in a girl with a heterozygous mutation in the ATRX Zn finger domain and a totally skewed X-inactivation pattern.

Authors :
Badens C
Martini N
Courrier S
DesPortes V
Touraine R
Levy N
Edery P
Source :
American journal of medical genetics. Part A [Am J Med Genet A] 2006 Oct 15; Vol. 140 (20), pp. 2212-5.
Publication Year :
2006

Abstract

Mutations in the X-encoded gene ATRX are known to give rise to syndromic mental retardation in male patients whereas female carriers show preferential inactivation of the mutated X chromosome and appear healthy. Here, we describe a 4-year-old girl with typical features of ATRX syndrome, carrying the recurrent R246C mutation of ATRX. We show that her pattern of X-inactivation is totally skewed and that her active X chromosome which harbors the ATRX mutation, was maternally inherited. To our knowledge, this is the first report of ATRX syndrome in a female patient. Since she was born after in vitro fertilization (IVF), we propose a possible link between assisted reproduction technologies (ART) and the unexpected X chromosome methylation pattern that we observed.<br /> ((c) 2006 Wiley-Liss, Inc.)

Details

Language :
English
ISSN :
1552-4825
Volume :
140
Issue :
20
Database :
MEDLINE
Journal :
American journal of medical genetics. Part A
Publication Type :
Academic Journal
Accession number :
16955409
Full Text :
https://doi.org/10.1002/ajmg.a.31400