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Genetic influences on mild mental retardation: concepts, findings and research implications

Published online by Cambridge University Press:  31 July 2008

Michael Rutter
Affiliation:
Social, Genetic and Developmental Psychiatry Research Centre, and MRC Child Psychiatry Unit, Institute of Psychiatry, De Crespigny Park, Denmark Hill, London SE5 8AF
Emily Simonoff
Affiliation:
Social, Genetic and Developmental Psychiatry Research Centre, and MRC Child Psychiatry Unit, Institute of Psychiatry, De Crespigny Park, Denmark Hill, London SE5 8AF
Robert Plomin
Affiliation:
Social, Genetic and Developmental Psychiatry Research Centre, and MRC Child Psychiatry Unit, Institute of Psychiatry, De Crespigny Park, Denmark Hill, London SE5 8AF

Extract

It has long been known that mild mental retardation (meaning that associated with an IQ in the 50–69 range) shows a strong tendency to run in families and that there is a much increased recurrence risk if either a parent or a sib has mental retardation. For example, Reed & Reed (1965) found that, having had one retarded child, the chance of a further retarded child was 6% if both parents and their sibs were ‘normal’, 13% if both parents were normal but one had a retarded sib, 20% if one parent was retarded, and 42% if both were retarded. A somewhat similar gradient was found in the more recent study by Bundey, Thake & Todd (1989). The appreciation that mild mental retardation was so strongly familial had led Lewis (1933) some years earlier to refer to it as ’subcultural‘ (meaning that it was a normal variation), in order to differentiate it from severe mental retardation, which was viewed as ‘pathological’. Penrose (1938, 1963) made the same classificatory distinction and the utility of a two-group approach became generally accepted (Burack, 1990).

Type
Session 3: Genetic Issues
Copyright
Copyright © Cambridge University Press 1996

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