Literature DB >> 12453600

Epilepsy in fragile X syndrome.

Gemma Incorpora1, Giovanni Sorge, Anna Sorge, Lorenzo Pavone.   

Abstract

The occurrence of seizures in patients with fragile X syndrome (Fra-X) is reported. Among the 30 patients, six had epilepsy that was particularly severe and two also showed atypical facial dysmorphism that was different from that seen in classical Fra-X. From the study performed in this series of Fra-X patients the authors arrived at the following conclusions. (1) The occurrence of seizures in Fra-X population is around 20%, as reported in the literature. (2) The EEG pattern of benign childhood epilepsy with central-temporal spikes (BCECTS) was found in only three patients (10%). (3) According to the pattern of seizures and EEGs, four groups may be recognizable, the less frequent being the uncommon group characterized by severe epilepsy unresponsive to treatment. (4) In this group atypical facial dysmorphism (although not similar in the two patients and different from the classical facial pattern of Fra-X) was found. The authors maintain that additional genetic factors might influence the clinical course and neurological aspects of Fra-X syndrome. Copyright 2002 Elsevier Science B.V.

Entities:  

Mesh:

Year:  2002        PMID: 12453600     DOI: 10.1016/s0387-7604(02)00102-x

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  19 in total

1.  The fragile X mutation impairs homeostatic plasticity in human neurons by blocking synaptic retinoic acid signaling.

Authors:  Zhenjie Zhang; Samuele G Marro; Yingsha Zhang; Kristin L Arendt; Christopher Patzke; Bo Zhou; Tyler Fair; Nan Yang; Thomas C Südhof; Marius Wernig; Lu Chen
Journal:  Sci Transl Med       Date:  2018-08-01       Impact factor: 17.956

2.  Altered neocortical rhythmic activity states in Fmr1 KO mice are due to enhanced mGluR5 signaling and involve changes in excitatory circuitry.

Authors:  Seth A Hays; Kimberly M Huber; Jay R Gibson
Journal:  J Neurosci       Date:  2011-10-05       Impact factor: 6.167

Review 3.  Modeling fragile X syndrome in the Fmr1 knockout mouse.

Authors:  Tatiana M Kazdoba; Prescott T Leach; Jill L Silverman; Jacqueline N Crawley
Journal:  Intractable Rare Dis Res       Date:  2014-11

Review 4.  Epilepsy and chromosomal abnormalities.

Authors:  Giovanni Sorge; Anna Sorge
Journal:  Ital J Pediatr       Date:  2010-05-03       Impact factor: 2.638

5.  Activity-dependent modulation of neural circuit synaptic connectivity.

Authors:  Charles R Tessier; Kendal Broadie
Journal:  Front Mol Neurosci       Date:  2009-07-30       Impact factor: 5.639

6.  Imbalance of neocortical excitation and inhibition and altered UP states reflect network hyperexcitability in the mouse model of fragile X syndrome.

Authors:  Jay R Gibson; Aundrea F Bartley; Seth A Hays; Kimberly M Huber
Journal:  J Neurophysiol       Date:  2008-09-10       Impact factor: 2.714

7.  Origins of epilepsy in fragile X syndrome.

Authors:  Paul J Hagerman; Carl E Stafstrom
Journal:  Epilepsy Curr       Date:  2009 Jul-Aug       Impact factor: 7.500

Review 8.  Fragile X syndrome: A review of clinical management.

Authors:  Reymundo Lozano; Atoosa Azarang; Tanaporn Wilaisakditipakorn; Randi J Hagerman
Journal:  Intractable Rare Dis Res       Date:  2016-08

Review 9.  Advances in the treatment of fragile X syndrome.

Authors:  Randi J Hagerman; Elizabeth Berry-Kravis; Walter E Kaufmann; Michele Y Ono; Nicole Tartaglia; Ave Lachiewicz; Rebecca Kronk; Carol Delahunty; David Hessl; Jeannie Visootsak; Jonathan Picker; Louise Gane; Michael Tranfaglia
Journal:  Pediatrics       Date:  2009-01       Impact factor: 7.124

Review 10.  The effects of early-life seizures on hippocampal dendrite development and later-life learning and memory.

Authors:  J R Casanova; Masataka Nishimura; John W Swann
Journal:  Brain Res Bull       Date:  2013-10-15       Impact factor: 4.077

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