Literature DB >> 21871821

Epilepsy in RAS/MAPK syndrome: two cases of cardio-facio-cutaneous syndrome with epileptic encephalopathy and a literature review.

Masao Adachi1, Yu Abe, Yoko Aoki, Yoichi Matsubara.   

Abstract

We report two individual cases of cardio-facio-cutaneous (CFC) syndrome with severe neurological impairment consisting of infantile spasms with hypsarrhythmia and refractory epilepsy with multifocal epileptic paroxysms such as modified hypsarrhythmia. Both cases shared diffuse brain atrophy and severely delayed myelination on neuroimaging. Genetic analysis revealed individual heterozygous mutations in the KRAS (phenotype of CFC/Noonan syndrome) and BRAF genes (phenotype of CFC syndrome). Neurological impairment in cases with mutations in the RAS/MAPK (mitogen activated protein kinase) signal pathway may be more severe, and could be linked to some forms of refractory epilepsy, especially epileptic encephalopathy that includes infantile spasms.
Copyright © 2011 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21871821     DOI: 10.1016/j.seizure.2011.07.013

Source DB:  PubMed          Journal:  Seizure        ISSN: 1059-1311            Impact factor:   3.184


  12 in total

Review 1.  Cardio-facio-cutaneous syndrome: clinical features, diagnosis, and management guidelines.

Authors:  Mary Ella M Pierpont; Pilar L Magoulas; Saleh Adi; Maria Ines Kavamura; Giovanni Neri; Jacqueline Noonan; Elizabeth I Pierpont; Kent Reinker; Amy E Roberts; Suma Shankar; Joseph Sullivan; Melinda Wolford; Brenda Conger; Molly Santa Cruz; Katherine A Rauen
Journal:  Pediatrics       Date:  2014-09-01       Impact factor: 7.124

2.  Assessing the gene-disease association of 19 genes with the RASopathies using the ClinGen gene curation framework.

Authors:  Andrew R Grant; Brandon J Cushman; Hélène Cavé; Mitchell W Dillon; Bruce D Gelb; Karen W Gripp; Jennifer A Lee; Heather Mason-Suares; Katherine A Rauen; Marco Tartaglia; Lisa M Vincent; Martin Zenker
Journal:  Hum Mutat       Date:  2018-11       Impact factor: 4.878

3.  Epilepsy in a cohort of children with Noonan syndrome and related disorders.

Authors:  Chiara Davico; Rossella D'Alessandro; Marta Borgogno; Filippa Campagna; Francesca Torta; Federica Ricci; Federico Amianto; Roberta Vittorini; Diana Carli; Alessandro Mussa; Benedetto Vitiello; Giovanni Battista Ferrero
Journal:  Eur J Pediatr       Date:  2022-05-16       Impact factor: 3.860

Review 4.  Latest American and European updates on infantile spasms.

Authors:  Andrew L Lux
Journal:  Curr Neurol Neurosci Rep       Date:  2013-03       Impact factor: 5.081

5.  Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosis.

Authors:  Karen W Gripp; Dina J Zand; Laurie Demmer; Carol E Anderson; William B Dobyns; Elaine H Zackai; Elizabeth Denenberg; Kim Jenny; Deborah L Stabley; Katia Sol-Church
Journal:  Am J Med Genet A       Date:  2013-08-05       Impact factor: 2.802

6.  Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene.

Authors:  Marianna Alagia; Pia Bernardo; Rita Genesio; Elena Gennaro; Nicola Brunetti-Pierri; Antonietta Coppola; Federico Zara; Pasquale Striano; Salvatore Striano; Gaetano Terrone
Journal:  Neurol Sci       Date:  2020-11-17       Impact factor: 3.307

7.  Identifying and Analyzing Novel Epilepsy-Related Genes Using Random Walk with Restart Algorithm.

Authors:  Wei Guo; Dong-Mei Shang; Jing-Hui Cao; Kaiyan Feng; Yi-Chun He; Yang Jiang; ShaoPeng Wang; Yu-Fei Gao
Journal:  Biomed Res Int       Date:  2017-02-01       Impact factor: 3.411

8.  Epileptic spasms in PPP1CB-associated Noonan-like syndrome: a case report with clinical and therapeutic implications.

Authors:  Chien-Heng Lin; Wei-De Lin; I-Ching Chou; Inn-Chi Lee; Hueng-Chuen Fan; Syuan-Yu Hong
Journal:  BMC Neurol       Date:  2018-09-20       Impact factor: 2.474

9.  Brain structural changes in patients with cardio-facio-cutaneous syndrome: effects of BRAF gene mutation and epilepsy on brain development. A case-control study by quantitative magnetic resonance imaging.

Authors:  Rosalinda Calandrelli; Fabio Pilato; Marco Panfili; Domenica Battaglia; Maria Luigia Gambardella; Cesare Colosimo
Journal:  Neuroradiology       Date:  2021-07-26       Impact factor: 2.804

10.  Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis.

Authors:  Hilary C Martin; Grace E Kim; Alistair T Pagnamenta; Yoshiko Murakami; Gemma L Carvill; Esther Meyer; Richard R Copley; Andrew Rimmer; Giulia Barcia; Matthew R Fleming; Jack Kronengold; Maile R Brown; Karl A Hudspith; John Broxholme; Alexander Kanapin; Jean-Baptiste Cazier; Taroh Kinoshita; Rima Nabbout; David Bentley; Gil McVean; Sinéad Heavin; Zenobia Zaiwalla; Tony McShane; Heather C Mefford; Deborah Shears; Helen Stewart; Manju A Kurian; Ingrid E Scheffer; Edward Blair; Peter Donnelly; Leonard K Kaczmarek; Jenny C Taylor
Journal:  Hum Mol Genet       Date:  2014-01-25       Impact factor: 6.150

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