Literature DB >> 19246929

Partial chromosome deletion: a new trisomy rescue mechanism?

F Vialard1, D Molina-Gomes, E Quarello, B Leroy, Y Ville, J Selva.   

Abstract

OBJECTIVE: We described a first case of a fetus with multiple congenital malformations associated with full trisomy 5 on direct CVS analysis and a partial trisomy 5 after cell culture.
METHODS: CVS karyotype (direct examination and culture) was performed after ultrasound examination and genetic counseling.
RESULTS: Direct CVS preparation showed a female karyotype with a homogeneous entire chromosome 5 trisomy, and karyotype of cultured CVS showed partial chromosome 5 trisomy, with an extra chromosome resulting from a deleted chromosome 5: 47,XX,del(5q31),+5. Only macroscopic examination could be performed because parents decided against postmortem examination and further analysis.
CONCLUSION: After a brief literature review, we argue that all de novo large chromosome deletions need to be considered as potentially associated with a trisomy rescue and uniparental disomy. (c) 2009 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2009        PMID: 19246929     DOI: 10.1159/000203400

Source DB:  PubMed          Journal:  Fetal Diagn Ther        ISSN: 1015-3837            Impact factor:   2.587


  2 in total

1.  Cytogenetic contribution to uniparental disomy (UPD).

Authors:  Thomas Liehr
Journal:  Mol Cytogenet       Date:  2010-03-29       Impact factor: 2.009

2.  Full trisomy 5 in a sample of spontaneous abortion and Arias Stella reaction.

Authors:  Vida Čulić; Bernarda Lozic; Ivana Kuzmić-Prusac; Goran Mijaljica; Jasminka Pavelić
Journal:  Med Sci Monit       Date:  2011-10
  2 in total

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