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The landscape of epilepsy-related GATOR1 variants
S. Baldassari, F. Picard, NE. Verbeek, M. van Kempen, EH. Brilstra, G. Lesca, V. Conti, R. Guerrini, F. Bisulli, L. Licchetta, T. Pippucci, P. Tinuper, E. Hirsch, A. de Saint Martin, J. Chelly, G. Rudolf, M. Chipaux, S. Ferrand-Sorbets, G....
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
682345
European Research Council - International
K12 NS098482
NINDS NIH HHS - United States
NLK
ProQuest Central
od 2011-01-01 do 2021-12-31
Health & Medicine (ProQuest)
od 2011-01-01 do 2021-12-31
ROAD: Directory of Open Access Scholarly Resources
od 1998
- MeSH
- Brugadův syndrom genetika mortalita patofyziologie MeSH
- dítě MeSH
- epilepsie komplikace epidemiologie genetika patofyziologie MeSH
- genetická predispozice k nemoci MeSH
- kojenec MeSH
- lidé MeSH
- mladiství MeSH
- mTORC1 genetika MeSH
- multiproteinové komplexy genetika MeSH
- mutace INDEL genetika MeSH
- mutace ztráty funkce genetika MeSH
- nádorové supresorové proteiny genetika MeSH
- novorozenec MeSH
- předškolní dítě MeSH
- proteiny aktivující GTPasu genetika MeSH
- represorové proteiny genetika MeSH
- rodokmen MeSH
- signální transdukce genetika MeSH
- variabilita počtu kopií segmentů DNA genetika MeSH
- záchvaty komplikace epidemiologie genetika patofyziologie MeSH
- Check Tag
- dítě MeSH
- kojenec MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- novorozenec MeSH
- předškolní dítě MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
PURPOSE: To define the phenotypic and mutational spectrum of epilepsies related to DEPDC5, NPRL2 and NPRL3 genes encoding the GATOR1 complex, a negative regulator of the mTORC1 pathway METHODS: We analyzed clinical and genetic data of 73 novel probands (familial and sporadic) with epilepsy-related variants in GATOR1-encoding genes and proposed new guidelines for clinical interpretation of GATOR1 variants. RESULTS: The GATOR1 seizure phenotype consisted mostly in focal seizures (e.g., hypermotor or frontal lobe seizures in 50%), with a mean age at onset of 4.4 years, often sleep-related and drug-resistant (54%), and associated with focal cortical dysplasia (20%). Infantile spasms were reported in 10% of the probands. Sudden unexpected death in epilepsy (SUDEP) occurred in 10% of the families. Novel classification framework of all 140 epilepsy-related GATOR1 variants (including the variants of this study) revealed that 68% are loss-of-function pathogenic, 14% are likely pathogenic, 15% are variants of uncertain significance and 3% are likely benign. CONCLUSION: Our data emphasize the increasingly important role of GATOR1 genes in the pathogenesis of focal epilepsies (>180 probands to date). The GATOR1 phenotypic spectrum ranges from sporadic early-onset epilepsies with cognitive impairment comorbidities to familial focal epilepsies, and SUDEP.
Bethel Epilepsy Centre Bielefeld Germany
Centre Hospitalier Universitaire de Rennes F 35000 Rennes France
CHU Reims American Memorial Hospital Service de Pédiatrie REIMS F 51092 France
CHU Reims Hôpital Maison Blanche Pôle de Biologie Service de Génétique Reims F 51092 France
Clinique Bernoise Crans Montana Switzerland
CNRS UMR 5292 INSERM U1028 CNRL et Université Claude Bernard Lyon 1 GHE Lyon France
Danish Epilepsy Centre Dianalund
Danish Epilepsy Centre Dianalund Denmark
Danish Epilepsy Centre Dianalund University of Copenhagen Copenhagen Denmark
Department of Biomedical and Neuromotor Sciences University of Bologna Bologna Italy
Department of Genetics University Medical Center Utrecht Utrecht The Netherlands
Department of Neurology Academic Center for Epileptology Kempenhaeghe Heeze The Netherlands
Department of Neurology and Rehabilitation Tallinn Children's Hospital Tallinn Estonia
Department of Pediatric Neurology Antwerp University Hospital Edegem Belgium
Department of Pediatric Neurosurgery Fondation Rothschild F 75019 Paris France
Department of Pediatrics Institute of Medicine University Hospital of Udine Udine Italy
Division of Genetics and Metabolism Phoenix Children's Hospital Phoenix Arizona USA
Epilepsy Center Clinic of Nervous System Diseases University of Foggia Riuniti Hospital Foggia Italy
Epilepsy Center for Children Brandenburg Medical School University Hospital Neuruppin Germany
IGBMC INSERM CNRS Strasbourg University Strasbourg France
Institut de Systématique Evolution Biodiversité ISYEB UMR 7205 CNRS MNHN UPMC EPHE Paris France
Institute for Regional Health research University of Southern Denmark Odense Denmark
Institute of Human Genetics University Hospital Magdeburg Germany
Institute of Human Genetics University of Leipzig Hospitals and Clinics Leipzig Germany
IRCCS Istituto delle Scienze Neurologiche of Bologna
Kinderneurologisches Zentrum Düsseldorf Gerresheim Sana Kliniken Düsseldorf Germany
Kingston Health Sciences Centre Kingston Ontario K7L 2V7 Canada
Leiden University Medical Center Leiden The Netherlands
Medical Genetics Unit Polyclinic Sant' Orsola Malpighi University Hospital Bologna Italy
Neurogenetics Group VIB Department of Molecular Genetics University of Antwerp Antwerp Belgium
Pediatric Neurology Department Timone Hospital APHM Marseille France
Service d'Epileptologie Clinique CHU de Bordeaux France
Service de Génétique Hospices Civils de Lyon GHE
Service de Génétique Médicale Pavillon Lefebvre Hôpital Purpan CHU Toulouse Toulouse France
Service de neurophysiologie et pédiatrie 1 CHU de Dijon Dijon France
Stichting Epilepsie Instellingen Nederland Zwolle Heemstede The Netherlands
The Saxon Epilepsy Center Kleinwachau Radeberg Germany
Unit of Medical Genetics CHU La Réunion Saint Pierre F 97448 France
Unité d'épileptologie Service de Neurologie CHU 49033 Angers France
Vrije Universiteit Brussel Neurogenetics Research Group Laarbeeklaan 101 1090 Brussels Belgium
Citace poskytuje Crossref.org
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- $a Baldassari, Sara $u Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France. INSERM, U1127, F-75013, Paris, France. CNRS, UMR 7225, F-75013, Paris, France. Institut du Cerveau et de la Moelle épinière (ICM), Hôpital Pitié-Salpêtrière, F-75013, Paris, France. Department of Genetics, Assistance Publique des Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, F-75013, Paris, France.
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- $a The landscape of epilepsy-related GATOR1 variants / $c S. Baldassari, F. Picard, NE. Verbeek, M. van Kempen, EH. Brilstra, G. Lesca, V. Conti, R. Guerrini, F. Bisulli, L. Licchetta, T. Pippucci, P. Tinuper, E. Hirsch, A. de Saint Martin, J. Chelly, G. Rudolf, M. Chipaux, S. Ferrand-Sorbets, G. Dorfmüller, S. Sisodiya, S. Balestrini, N. Schoeler, L. Hernandez-Hernandez, S. Krithika, R. Oegema, E. Hagebeuk, B. Gunning, C. Deckers, B. Berghuis, I. Wegner, E. Niks, FE. Jansen, K. Braun, D. de Jong, G. Rubboli, I. Talvik, V. Sander, P. Uldall, ML. Jacquemont, C. Nava, E. Leguern, S. Julia, A. Gambardella, G. d'Orsi, G. Crichiutti, L. Faivre, V. Darmency, B. Benova, P. Krsek, A. Biraben, AS. Lebre, M. Jennesson, S. Sattar, C. Marchal, DR. Nordli, K. Lindstrom, P. Striano, LB. Lomax, C. Kiss, F. Bartolomei, AF. Lepine, AS. Schoonjans, K. Stouffs, A. Jansen, E. Panagiotakaki, B. Ricard-Mousnier, J. Thevenon, J. de Bellescize, H. Catenoix, T. Dorn, M. Zenker, K. Müller-Schlüter, C. Brandt, I. Krey, T. Polster, M. Wolff, M. Balci, K. Rostasy, G. Achaz, P. Zacher, T. Becher, T. Cloppenborg, CJ. Yuskaitis, S. Weckhuysen, A. Poduri, JR. Lemke, RS. Møller, S. Baulac,
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- 700 1_
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- 700 1_
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- $a Baulac, Stéphanie $u Sorbonne Université, UPMC Univ Paris 06, UMR S 1127, F-75013, Paris, France. stephanie.baulac@upmc.fr. INSERM, U1127, F-75013, Paris, France. stephanie.baulac@upmc.fr. CNRS, UMR 7225, F-75013, Paris, France. stephanie.baulac@upmc.fr. Institut du Cerveau et de la Moelle épinière (ICM), Hôpital Pitié-Salpêtrière, F-75013, Paris, France. stephanie.baulac@upmc.fr. Department of Genetics, Assistance Publique des Hôpitaux de Paris (AP-HP), Hôpital Pitié-Salpêtrière, F-75013, Paris, France. stephanie.baulac@upmc.fr.
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