Volume 74, Issue 5 pp. 515-520
Research Article
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A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8

Ingrid Claeys

Ingrid Claeys

Department of Pediatrics, University Hospital Leuven, Leuven, Belgium

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Maureen Holvoet

Maureen Holvoet

Center for Human Genetics, University Hospital Leuven, Leuven, Belgium

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Benedicte Eyskens

Benedicte Eyskens

Department of Pediatric Cardiology Unit, University Hospital Leuven, Leuven, Belgium

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Peter Adriaensens

Peter Adriaensens

Department of Children's Psychiatry, University Hospital Leuven, Leuven, Belgium

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Marc Gewillig

Marc Gewillig

Department of Pediatric Cardiology Unit, University Hospital Leuven, Leuven, Belgium

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Jean-Pierre Fryns

Jean-Pierre Fryns

Center for Human Genetics, University Hospital Leuven, Leuven, Belgium

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Koenraad Devriendt

Corresponding Author

Koenraad Devriendt

Center for Human Genetics, University Hospital Leuven, Leuven, Belgium

Center for Human Genetics, Herestraat 49, B-3000 Leuven, BelgiumSearch for more papers by this author

Abstract

We report the clinical findings in 5 patients with a terminal deletion of the short arm of chromosome 8. Mild developmental delay was constantly present, in association with microcephaly in 4 of 5 patients. Facial anomalies were mild or absent. A congenital heart defect was present in 3 patients: an atrioventricular septal defect (AVSD) in 2 and an atrial septal defect type II (ASDII) with pulmonary stenosis in one. A highly similar pattern of behavioural difficulties was present in the 3 older children (8–11 years), with outbursts of aggressiveness and destructive behaviour. Follow-up in one patient showed that at the age of 16 years, these behavioural problems had largely disappeared. This observation suggests that in addition to mental retardation, microcephaly, congenital heart defect (typically AVSD), a terminal deletion of chromosome 8p may be associated with a characteristic behavioural phenotype during childhood. Am. J. Med. Genet. 74:515–520, 1997. © 1997 Wiley-Liss, Inc.

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