Literature DB >> 9342203

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8.

I Claeys1, M Holvoet, B Eyskens, P Adriaensens, M Gewillig, J P Fryns, K Devriendt.   

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.

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Year:  1997        PMID: 9342203     DOI: 10.1002/(sici)1096-8628(19970919)74:5<515::aid-ajmg12>3.0.co;2-f

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  13 in total

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3.  Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.

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Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

4.  The general anesthesia experience of deletion 8p syndrome patient -A case report-.

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5.  Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks.

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Journal:  Am J Med Genet A       Date:  2012-11-19       Impact factor: 2.802

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Journal:  Behav Genet       Date:  2011-01-23       Impact factor: 2.805

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Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

8.  Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

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Journal:  J Pediatr Genet       Date:  2015-10-14

Review 9.  Chromosomal phenotypes and submicroscopic abnormalities.

Authors:  Koen Devriendt; Joris R Vermeesch
Journal:  Hum Genomics       Date:  2004-01       Impact factor: 4.639

Review 10.  Multifaceted Regulation of MicroRNA Biogenesis: Essential Roles and Functional Integration in Neuronal and Glial Development.

Authors:  Izabela Suster; Yue Feng
Journal:  Int J Mol Sci       Date:  2021-06-23       Impact factor: 5.923

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