Literature DB >> 24623842

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.

Gemma L Carvill1, Sarah Weckhuysen, Jacinta M McMahon, Corinna Hartmann, Rikke S Møller, Helle Hjalgrim, Joseph Cook, Eileen Geraghty, Brian J O'Roak, Steve Petrou, Alison Clarke, Deepak Gill, Lynette G Sadleir, Hiltrud Muhle, Sarah von Spiczak, Marina Nikanorova, Bree L Hodgson, Elena V Gazina, Arvid Suls, Jay Shendure, Leanne M Dibbens, Peter De Jonghe, Ingo Helbig, Samuel F Berkovic, Ingrid E Scheffer, Heather C Mefford.   

Abstract

OBJECTIVE: To determine the genes underlying Dravet syndrome in patients who do not have an SCN1A mutation on routine testing.
METHODS: We performed whole-exome sequencing in 13 SCN1A-negative patients with Dravet syndrome and targeted resequencing in 67 additional patients to identify new genes for this disorder.
RESULTS: We detected disease-causing mutations in 2 novel genes for Dravet syndrome, with mutations in GABRA1 in 4 cases and STXBP1 in 3. Furthermore, we identified 3 patients with previously undetected SCN1A mutations, suggesting that SCN1A mutations occur in even more than the currently accepted ∼ 75% of cases.
CONCLUSIONS: We show that GABRA1 and STXBP1 make a significant contribution to Dravet syndrome after SCN1A abnormalities have been excluded. Our results have important implications for diagnostic testing, clinical management, and genetic counseling of patients with this devastating disorder and their families.

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Year:  2014        PMID: 24623842      PMCID: PMC4001207          DOI: 10.1212/WNL.0000000000000291

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  36 in total

1.  Association of genomic deletions in the STXBP1 gene with Ohtahara syndrome.

Authors:  H Saitsu; M Kato; M Shimono; A Senju; S Tanabe; T Kimura; K Nishiyama; Y Yoneda; Y Kondo; Y Tsurusaki; H Doi; N Miyake; K Hayasaka; N Matsumoto
Journal:  Clin Genet       Date:  2011-12-28       Impact factor: 4.438

2.  A novel STXBP1 mutation causes focal seizures with neonatal onset.

Authors:  Matteo Vatta; Michael B Tennison; Arthur S Aylsworth; Christie M Turcott; Maria P Guerra; Christine M Eng; Yaping Yang
Journal:  J Child Neurol       Date:  2012-06       Impact factor: 1.987

3.  STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients.

Authors:  Cyril Mignot; Marie-Laure Moutard; Oriane Trouillard; Isabelle Gourfinkel-An; Aurélia Jacquette; Benoit Arveiler; Fanny Morice-Picard; Didier Lacombe; Catherine Chiron; Dorothée Ville; Perrine Charles; Eric LeGuern; Christel Depienne; Delphine Héron
Journal:  Epilepsia       Date:  2011-07-18       Impact factor: 5.864

4.  Targeted next generation sequencing as a diagnostic tool in epileptic disorders.

Authors:  Johannes R Lemke; Erik Riesch; Tim Scheurenbrand; Max Schubach; Christian Wilhelm; Isabelle Steiner; Jörg Hansen; Carolina Courage; Sabina Gallati; Sarah Bürki; Susi Strozzi; Barbara Goeggel Simonetti; Sebastian Grunt; Maja Steinlin; Michael Alber; Markus Wolff; Thomas Klopstock; Eva C Prott; Rüdiger Lorenz; Christiane Spaich; Sabine Rona; Maya Lakshminarasimhan; Judith Kröll; Thomas Dorn; Günter Krämer; Matthis Synofzik; Felicitas Becker; Yvonne G Weber; Holger Lerche; Detlef Böhm; Saskia Biskup
Journal:  Epilepsia       Date:  2012-05-21       Impact factor: 5.864

5.  A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome.

Authors:  Ikuo Ogiwara; Tojo Nakayama; Tetsushi Yamagata; Hideyuki Ohtani; Emi Mazaki; Shigeru Tsuchiya; Yushi Inoue; Kazuhiro Yamakawa
Journal:  Epilepsia       Date:  2012-11-13       Impact factor: 5.864

6.  Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations.

Authors:  Mathieu Milh; Nathalie Villeneuve; Mondher Chouchane; Anna Kaminska; Cécile Laroche; Marie Anne Barthez; Cyril Gitiaux; Céline Bartoli; Ana Borges-Correia; Pierre Cacciagli; Cécile Mignon-Ravix; Hélène Cuberos; Brigitte Chabrol; Laurent Villard
Journal:  Epilepsia       Date:  2011-07-19       Impact factor: 5.864

7.  Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers.

Authors:  Sarah Weckhuysen; Philip Holmgren; Rik Hendrickx; Anna C Jansen; Daniele Hasaerts; Charlotte Dielman; Julitta de Bellescize; Nadia Boutry-Kryza; Gaetan Lesca; Sarah Von Spiczak; Ingo Helbig; Deepak Gill; Simone Yendle; Rikke S Møller; Laura Klitten; Christian Korff; Catherine Godfraind; Kenou Van Rijckevorsel; Peter De Jonghe; Helle Hjalgrim; Ingrid E Scheffer; Arvid Suls
Journal:  Epilepsia       Date:  2013-02-14       Impact factor: 5.864

8.  Do mutations in SCN1B cause Dravet syndrome?

Authors:  Young Ok Kim; Leanne Dibbens; Carla Marini; Arvid Suls; Nicole Chemaly; Davide Mei; Jacinta M McMahon; Xenia Iona; Samuel F Berkovic; Peter De Jonghe; Renzo Guerrini; Rima Nabbout; Ingrid E Scheffer
Journal:  Epilepsy Res       Date:  2012-11-20       Impact factor: 3.045

9.  Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

Authors:  Brian J O'Roak; Laura Vives; Wenqing Fu; Jarrett D Egertson; Ian B Stanaway; Ian G Phelps; Gemma Carvill; Akash Kumar; Choli Lee; Katy Ankenman; Jeff Munson; Joseph B Hiatt; Emily H Turner; Roie Levy; Diana R O'Day; Niklas Krumm; Bradley P Coe; Beth K Martin; Elhanan Borenstein; Deborah A Nickerson; Heather C Mefford; Dan Doherty; Joshua M Akey; Raphael Bernier; Evan E Eichler; Jay Shendure
Journal:  Science       Date:  2012-11-15       Impact factor: 47.728

10.  Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

Authors:  Gemma L Carvill; Sinéad B Heavin; Simone C Yendle; Jacinta M McMahon; Brian J O'Roak; Joseph Cook; Adiba Khan; Michael O Dorschner; Molly Weaver; Sophie Calvert; Stephen Malone; Geoffrey Wallace; Thorsten Stanley; Ann M E Bye; Andrew Bleasel; Katherine B Howell; Sara Kivity; Mark T Mackay; Victoria Rodriguez-Casero; Richard Webster; Amos Korczyn; Zaid Afawi; Nathanel Zelnick; Tally Lerman-Sagie; Dorit Lev; Rikke S Møller; Deepak Gill; Danielle M Andrade; Jeremy L Freeman; Lynette G Sadleir; Jay Shendure; Samuel F Berkovic; Ingrid E Scheffer; Heather C Mefford
Journal:  Nat Genet       Date:  2013-05-26       Impact factor: 38.330

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  88 in total

1.  Synaptopathies Heat Up: Mutations in STX1B in Fever-Associated Epilepsies.

Authors:  Jennifer A Kearney
Journal:  Epilepsy Curr       Date:  2015 May-Jun       Impact factor: 7.500

2.  Clinical Genetic Testing in Epilepsy.

Authors:  Heather C Mefford
Journal:  Epilepsy Curr       Date:  2015 Jul-Aug       Impact factor: 7.500

Review 3.  Ionotropic GABA and Glutamate Receptor Mutations and Human Neurologic Diseases.

Authors:  Hongjie Yuan; Chian-Ming Low; Olivia A Moody; Andrew Jenkins; Stephen F Traynelis
Journal:  Mol Pharmacol       Date:  2015-04-22       Impact factor: 4.436

4.  Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder.

Authors:  Noa Lipstein; Nanda M Verhoeven-Duif; Francesco E Michelassi; Nathaniel Calloway; Peter M van Hasselt; Katarzyna Pienkowska; Gijs van Haaften; Mieke M van Haelst; Ron van Empelen; Inge Cuppen; Heleen C van Teeseling; Annemieke M V Evelein; Jacob A Vorstman; Sven Thoms; Olaf Jahn; Karen J Duran; Glen R Monroe; Timothy A Ryan; Holger Taschenberger; Jeremy S Dittman; Jeong-Seop Rhee; Gepke Visser; Judith J Jans; Nils Brose
Journal:  J Clin Invest       Date:  2017-02-13       Impact factor: 14.808

Review 5.  The genetics of the epilepsies.

Authors:  Christelle M El Achkar; Heather E Olson; Annapurna Poduri; Phillip L Pearl
Journal:  Curr Neurol Neurosci Rep       Date:  2015-07       Impact factor: 5.081

6.  A missense mutation in SLC6A1 associated with Lennox-Gastaut syndrome impairs GABA transporter 1 protein trafficking and function.

Authors:  Kefu Cai; Jie Wang; Jaclyn Eissman; Juexin Wang; Gerald Nwosu; Wangzhen Shen; Hui-Ci Liang; Xiao-Jing Li; Hai-Xia Zhu; Yong-Hong Yi; Jeffrey Song; Dong Xu; Eric Delpire; Wei-Ping Liao; Yi-Wu Shi; Jing-Qiong Kang
Journal:  Exp Neurol       Date:  2019-06-06       Impact factor: 5.330

7.  De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies.

Authors: 
Journal:  Am J Hum Genet       Date:  2014-09-25       Impact factor: 11.025

Review 8.  Defects at the crossroads of GABAergic signaling in generalized genetic epilepsies.

Authors:  Jing-Qiong Kang
Journal:  Epilepsy Res       Date:  2017-08-26       Impact factor: 3.045

9.  Altered inhibitory synapses in de novo GABRA5 and GABRA1 mutations associated with early onset epileptic encephalopathies.

Authors:  Ciria C Hernandez; Wenshu XiangWei; Ningning Hu; Dingding Shen; Wangzhen Shen; Andre H Lagrange; Yujia Zhang; Lifang Dai; Changhong Ding; Zhaohui Sun; Jiasheng Hu; Hongmin Zhu; Yuwu Jiang; Robert L Macdonald
Journal:  Brain       Date:  2019-07-01       Impact factor: 13.501

10.  Epileptic encephalopathy de novo GABRB mutations impair γ-aminobutyric acid type A receptor function.

Authors:  Vaishali S Janve; Ciria C Hernandez; Kelienne M Verdier; Ningning Hu; Robert L Macdonald
Journal:  Ann Neurol       Date:  2016-05       Impact factor: 10.422

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