Format

Send to

Choose Destination
See comment in PubMed Commons below
Clin Genet. 1998 May;53(5):408-10.

Deletion in chromosome region 22q11 in a child with CHARGE association.

Author information

1
Center for Human Genetics, University Hospital Leuven, Belgium. koen.devriendt@med.kuleuven.ac.be

Abstract

We present a female child with features of the CHARGE association, including iris coloboma, large ventricular septum defect (VSD), external ear abnormalities, severe growth retardation and moderate mental delay. A submicroscopic deletion in chromsome 22q11 was detected by means of fluorescence in situ hybridization (FISH) using probe DO832. The clinical features in this child compromise characteristics of both the velo-cardio-facial syndrome (VCFS) and the cat-eye syndrome. This may suggest the presence of a more complex rearrangement of 22q, with a deletion-duplication.

PMID:
9660062
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments

    Supplemental Content

    Full text links

    Icon for Wiley
    Loading ...
    Support Center