Literature DB >> 20864408

Potential therapeutic interventions for fragile X syndrome.

Josien Levenga1, Femke M S de Vrij, Ben A Oostra, Rob Willemsen.   

Abstract

Fragile X syndrome (FXS) is caused by a lack of the fragile X mental retardation protein (FMRP); FMRP deficiency in neurons of patients with FXS causes intellectual disability (IQ<70) and several behavioural problems, including hyperactivity and autistic-like features. In the brain, no gross morphological malformations have been found, although subtle spine abnormalities have been reported. FXS has been linked to altered group I metabotropic glutamate receptor (mGluR)-dependent and independent forms of synaptic plasticity. Here, we discuss potential targeted therapeutic strategies developed to specifically correct disturbances in the excitatory mGluR and the inhibitory gamma-aminobutyric (GABA) receptor pathways that have been tested in animal models and/or in clinical trials with patients with FXS.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20864408      PMCID: PMC2981507          DOI: 10.1016/j.molmed.2010.08.005

Source DB:  PubMed          Journal:  Trends Mol Med        ISSN: 1471-4914            Impact factor:   11.951


  108 in total

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  31 in total

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3.  Real-Time Imaging Reveals Properties of Glutamate-Induced Arc/Arg 3.1 Translation in Neuronal Dendrites.

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