A Recognisable Behavioural Phenotype Associated with Terminal Deletions of the Short Arm of Chromosome 8
Overview
Affiliations
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.
Yasuhara J, Garg V Transl Pediatr. 2021; 10(9):2366-2386.
PMID: 34733677 PMC: 8506053. DOI: 10.21037/tp-21-297.
Suster I, Feng Y Int J Mol Sci. 2021; 22(13).
PMID: 34201807 PMC: 8269442. DOI: 10.3390/ijms22136765.
Wagner-Mahler K, Kurzenne J, Gastaud F, Hoflack M, Panaia Ferrari P, Berard E Mol Genet Genomic Med. 2019; 7(3):e558.
PMID: 30690934 PMC: 6418366. DOI: 10.1002/mgg3.558.
Pierpont M, Brueckner M, Chung W, Garg V, Lacro R, McGuire A Circulation. 2018; 138(21):e653-e711.
PMID: 30571578 PMC: 6555769. DOI: 10.1161/CIR.0000000000000606.
Shi S, Lin S, Chen B, Zhou Y Mol Med Rep. 2017; 16(5):6837-6845.
PMID: 28901431 PMC: 5865842. DOI: 10.3892/mmr.2017.7438.