Reference : Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic...
Scientific journals : Article
Life sciences : Genetics & genetic processes
Systems Biomedicine
http://hdl.handle.net/10993/42973
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy
English
Chatron, Nicolas []
Becker, Felicitas []
Morsy, Herba []
Schmidts, Miriam []
Hardies, Katia []
Tuysuz, Beyhan []
Roselli, Sandra []
Najafi, Maryam []
Alkaya, Dilek Uludag []
Ashrafzadeh, Farah []
Nabil, Amira []
Omar, Turek []
Maroofian, Reza []
Karimiani, Ehsan Ghayoor []
Hussein, Haytham []
Kok, Fernando []
Ramos, Luiza []
Gunes, Nilay []
Bilguvar, Kaya []
Labalme, Audrey []
Alix, Eudeline []
Sanlaville, Damien []
De Bellescize, Julitta []
Poulat, Anne-Lise []
EuroEPINOMICS-RES consrtium AR working group []
Moslemi, Ali-Reza []
Lerche, Holger []
May, Patrick mailto [University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB) > >]
Lesca, Gaetan []
Weckhuysen, Sarah []
Tajsharghi, Homa []
13-Apr-2020
Brain: a Journal of Neurology
Oxford University Press
Yes (verified by ORBilu)
International
0006-8950
1460-2156
Oxford
United Kingdom
[en] Epilepsy ; GAD1 ; Developmental Syndrome ; Suppression-burs ; Hypsarrhythmia ; arthrogryposis ; omphalocele ; cleft palate
[en] Developmental and Epileptic Encephalopathies are a heterogeneous group of early-onset epilepsy syndromes dramatically impairing neurodevelopment. Modern genomic technologies have revealed a number of monogenic origins and opened the door to therapeutic hopes. Here we describe a new syndromic developmental and epileptic encephalopathies caused by bi-allelic loss of function variants in GAD1, as presented by eleven patients from 6 independent consanguineous families. Seizure onset occurred in the two first months of life in all patients. All 10 patients from whom early disease history was available, presented seizure onset in the first month of life, mainly consisting of epileptic spasms or myoclonic seizures. Early electroencephalography showed suppression-burst or pattern of burst attenuation or hypsarrhythmia if only recorded in the post-neonatal period. Eight patients had joint contractures and/or pes equinovarus. Seven patients presented a cleft palate and two also had an omphalocele, reproducing the phenotype of the knockout Gad1-/- mouse model. Four patients died before four years of age. GAD1 encodes the glutamate decarboxylase enzyme GAD67, a critical actor of the γ-aminobutyric acid (GABA) metabolism as it catalyzes the decarboxylation of glutamic acid to form GABA. Our findings evoke a novel syndrome related to GAD67 deficiency, characterized by the unique association of developmental and epileptic encephalopathies, cleft palate, joint contractures and/or omphalocele.
Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) ; University of Luxembourg: High Performance Computing - ULHPC
Researchers
http://hdl.handle.net/10993/42973
10.1093/brain/awaa085
https://academic.oup.com/brain/article/doi/10.1093/brain/awaa085/5819590

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