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Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3.

Authors :
Tzschach A
Hoeltzenbein M
Hoffmann K
Menzel C
Beyer A
Ocker V
Wurster G
Raynaud M
Ropers HH
Kalscheuer V
Heilbronner H
Source :
European journal of human genetics : EJHG [Eur J Hum Genet] 2006 Dec; Vol. 14 (12), pp. 1317-20. Date of Electronic Publication: 2006 Aug 23.
Publication Year :
2006

Abstract

We report on a 2-year-old girl with situs ambiguus comprising right-sided stomach and spleen, left-sided liver and complex cardiac defect. Psychomotor development of this patient was normal, and no other major abnormalities were present. Chromosome analysis revealed a de novo balanced chromosome translocation t(X;1)(q26;p13.1). Molecular cytogenetic investigations identified a breakpoint spanning BAC clone on the X-chromosome containing the ZIC3 gene. Mutations in ZIC3 are associated with situs ambiguus and cardiac defects predominantly in males. This is the first report of a live born girl with an X-autosome translocation involving the ZIC3 region.

Details

Language :
English
ISSN :
1018-4813
Volume :
14
Issue :
12
Database :
MEDLINE
Journal :
European journal of human genetics : EJHG
Publication Type :
Academic Journal
Accession number :
16926859
Full Text :
https://doi.org/10.1038/sj.ejhg.5201707