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Ring-X chromosomes: their cognitive and behavioural phenotype

Published online by Cambridge University Press:  26 July 2016

J. KUNTSI
Affiliation:
Behavioural Sciences Unit, Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK
D. SKUSE
Affiliation:
Behavioural Sciences Unit, Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK
K. ELGAR
Affiliation:
Behavioural Sciences Unit, Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK
E. MORRIS
Affiliation:
Behavioural Sciences Unit, Institute of Child Health, University College London, 30 Guilford Street, London WC1N 1EH, UK
C. TURNER
Affiliation:
Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire SP2 8BJ, UK
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Abstract

We tested the cognitive abilities and educational attainments of 47 patients with a ring X chromosome, to evaluate the extent to which these variables correlated with failure of r(X) inactivation and with mosaicism. We found possession of a r(X) chromosome was associated with an increased risk of significant learning difficulties, and with associated behavioural maladjustment, compared with 45,X Turner females. Nearly a third had been educated outside mainstream schools. The proportion of cells in peripheral blood containing an inactivated r(X) chromosome was negatively correlated with nonverbal IQ. The parental origin of the normal chromosome did not appear to affect adjustment or abilities. In a minority of r(X) cases associated with mental retardation, there had been a failure to inactivate the ring, due to loss of the XIST locus. However, failure of X-inactivation was not necessarily associated with a severe phenotype. The degree of impairment in IQ depended on the size of the active ring, and hence was proportionate to the number of (as yet unidentified) genes whose functional disomy affected brain development and functioning.

Type
Research Article
Copyright
University College London 2000

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