Monozygotic boys with fragile X syndrome.

Abstract:

:Monozygotic twin boys with fragile X syndrome underwent thorough genetic, psychiatric, neurological, and language evaluations at 10 years of age. They both demonstrated physical features, speech and language difficulties, social problems, and attentional deficits that characterize the behavioural phenotype of fragile X syndrome. Despite identical genetic constitutions, there were important developmental and behavioural heterogeneities. Twin A showed less social interaction and symbolic play and more speech and language dysfunction than twin B. Twin A also had significantly larger caudate volumes. It is suggested that the Xq27.3 anomaly may not be sufficient to account for all the behavioural phenotypic and neuroanatomical features of fragile X syndrome.

journal_name

Dev Med Child Neurol

authors

Sheldon L,Turk J

doi

10.1017/s0012162200001420

subject

Has Abstract

pub_date

2000-11-01 00:00:00

pages

768-74

issue

11

eissn

0012-1622

issn

1469-8749

journal_volume

42

pub_type

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