Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter.
Livio Pagano, G Fioretti, M Vetrella, E Risolo, C Casullo, Antonio Celona, S Renda, A Rinaldi, V. Ventruto
Abstract
Livio Pagano, G Fioretti, M Vetrella, E Risolo, C Casullo, Antonio Celona, S Renda, A Rinaldi, V. Ventruto
Abstract
The authors report on a family with a t(3;6). All four members of a sibship were carriers of the balanced translocation and two have had children with multiple malformations. The proband, six months old, had the karyotype 46,XY, t(3;6) (p26;p21) der pat. His clinical features were typical of the trisomy 6p syndrome. HLA typing data failed demonstrate both paternal haplotypes in the propositus.
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The authors report on a family with a t(3;6). All four members of a sibship were carriers of the balanced translocation and two have had children with multiple malformations. The proband, six months old, had the karyotype 46,XY, t(3;6) (p26;p21) der pat. His clinical features were typical of the trisomy 6p syndrome. HLA typing data failed demonstrate both paternal haplotypes in the propositus.
Key concepts: Chromosomal translocation, Proband, Biology, Partial Trisomy, Karyotype, Genetics, Trisomy, Congenital malformations