Neurodevelopmental effects of the FMR-1 full mutation in humans

Allan L. Reiss, Michael T. Abrams, Ronald Greenlaw, Lisa Freund, Martha B. Denckla

Research output: Contribution to journalArticle

Abstract

Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability. Using magnetic resonance imaging (MRI) and quantitative morphometry, we have compared the neuroanatomy of 51 individuals with an FMR-1 mutation with matched controls and showed that subjects with an FMR-1 mutation have increased volume of the caudate nucleus and, in males, the lateral ventricle. Both caudate and lateral ventricular volumes are correlated with IQ. Caudate volume is also correlated with the methylation status of the FMR-1 gene. Neuroanatom-ical differences between two monozygotic twins with an FMR-1 mutation who are discordant for mental retardation are localized to the cerebellum, lateral ventricles and subcortical nuclei. These findings suggest that the FMR-1 mutation causing the fragile X syndrome leads to observable changes in neuroanatomy that may be relevant to the neurodevelopmental disability and behavioural problems observed in affected individuals.

Original languageEnglish (US)
Pages (from-to)159-167
Number of pages9
JournalNature medicine
Volume1
Issue number2
DOIs
StatePublished - Feb 1995

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Fingerprint Dive into the research topics of 'Neurodevelopmental effects of the FMR-1 full mutation in humans'. Together they form a unique fingerprint.

  • Cite this