| Literature DB >> 11940088 |
D Sanlaville1, S P Romana, J M Lapierre, J Amiel, D Genevieve, C Ozilou, M Le Lorch, S Brisset, P Gosset, C Baumann, C Turleau, S Lyonnet, M Vekemans.
Abstract
CHARGE association is a non-random occurrence of congenital malformations including coloboma, heart disease, choanal atresia, retarded growth and/or retarded development, genital hypoplasia, ear anomalies and/or deafness. The cause of this association remains unknown. Various genetic mechanisms have been proposed, including a contiguous gene syndrome but, so far, no recurrent locus has been identified. To address this question, we decided to perform a comparative genomic hybridization (CGH) study on a cohort of 27 patients with CHARGE association and a normal standard karyotype. We found two chromosomal anomalies: a der(9)t(9;13) derived from a paternal translocation and a der(6)t(4;6) of unknown origin. This suggests that chromosome imbalances may well mimic CHARGE association. Therefore patients with CHARGE association must be carefully tested with classical and molecular cytogenetic techniques to detect a potential chromosome imbalance. It is expected that more stringent diagnostic criteria of CHARGE association could define a more homogeneous group of patients where a single genetic cause might be identified.Entities:
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Year: 2002 PMID: 11940088 DOI: 10.1034/j.1399-0004.2002.610208.x
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438