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

Journal: European Journal Of Human Genetics : EJHG
Published:
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.

Authors
Andreas Tzschach, Maria Hoeltzenbein, Kirsten Hoffmann, Corinna Menzel, Alexander Beyer, Volker Ocker, Goetz Wurster, Martine Raynaud, Hans-hilger Ropers, Vera Kalscheuer, Helmut Heilbronner