OBJECTIVE: To find the length and location of the deletions in the short arm of chromosome 5 in one case of Cri du Chat syndrome using oligo array comparative genomic hybridization. METHODS: Metaphase chromosomes were prepared from peripheral blood lymphocyte cultures using standard cytogenetic protocols. Chromosomal analysis was done in G-banded metaphases. Oligo array comparative genomic hybridization and fluorescence in situ hybridization were performed by the commercially available kits. RESULTS: Oligonucleotide array comparative genomic hybridization (CGH) analysis revealed a 23.263 Mb deletion at region 5p14.2-->qter, combined with a duplication of 14.602 Mb in size in the area 12p13.1-->pter. Chromosomal aberrations were confirmed by fluorescence in situ hybridization. The male neonate with Cri du Chat syndrome had an unbalanced translocation which was inherited from his father who was a balanced carrier with a karyotype 46, XY, t (5; 12) (p14.2; p13.1). CONCLUSIONS: This report shows the clinical utility of the oligonucleotide array in the detection of submicroscopic chromosomal aberrations, thus improving the molecular diagnosis of Cri du Chat syndrome.
OBJECTIVE: To find the length and location of the deletions in the short arm of chromosome 5 in one case of Cri du Chat syndrome using oligo array comparative genomic hybridization. METHODS: Metaphase chromosomes were prepared from peripheral blood lymphocyte cultures using standard cytogenetic protocols. Chromosomal analysis was done in G-banded metaphases. Oligo array comparative genomic hybridization and fluorescence in situ hybridization were performed by the commercially available kits. RESULTS:Oligonucleotide array comparative genomic hybridization (CGH) analysis revealed a 23.263 Mb deletion at region 5p14.2-->qter, combined with a duplication of 14.602 Mb in size in the area 12p13.1-->pter. Chromosomal aberrations were confirmed by fluorescence in situ hybridization. The male neonate with Cri du Chat syndrome had an unbalanced translocation which was inherited from his father who was a balanced carrier with a karyotype 46, XY, t (5; 12) (p14.2; p13.1). CONCLUSIONS: This report shows the clinical utility of the oligonucleotide array in the detection of submicroscopic chromosomal aberrations, thus improving the molecular diagnosis of Cri du Chat syndrome.
Authors: A L Mosca; P Callier; B Leheup; N Marle; M Jalloul; L Coffinet; F Feillet; M Valduga; P Jonveaux; F Mugneret Journal: Am J Med Genet A Date: 2007-06-15 Impact factor: 2.802
Authors: M Vlckova; M Trkova; Z Zemanova; M Hancarova; D Novotna; D Raskova; A Puchmajerova; J Drabova; Z Zmitkova; Y Tan; Z Sedlacek Journal: Cytogenet Genome Res Date: 2011-12-08 Impact factor: 1.636
Authors: Sarah T South; Jeffrey J Swensen; Teresa Maxwell; Alan Rope; Arthur R Brothman; Zhong Chen Journal: Am J Med Genet A Date: 2006-12-15 Impact factor: 2.802