نتایج جستجو برای: early infantile epileptic encephalopathy

تعداد نتایج: 725871  

2015
Isabelle Thiffault David J. Speca Daniel C. Austin Melanie M. Cobb Kenneth S. Eum Nicole P. Safina Lauren Grote Emily G. Farrow Neil Miller Sarah Soden Stephen F. Kingsmore James S. Trimmer Carol J. Saunders Jon T. Sack

The epileptic encephalopathies are a group of highly heterogeneous genetic disorders. The majority of disease-causing mutations alter genes encoding voltage-gated ion channels, neurotransmitter receptors, or synaptic proteins. We have identified a novel de novo pathogenic K+ channel variant in an idiopathic epileptic encephalopathy family. Here, we report the effects of this mutation on channel...

Journal: :Developmental medicine and child neurology 2011
Jehan Suleiman Tanja Brenner Deepak Gill Christopher Troedson Adriane J Sinclair Fabienne Brilot Angela Vincent Bethan Lang Russell C Dale

Autoantibodies that bind to voltage-gated potassium-channel complex proteins (VGKC-complex antibodies) occur frequently in adults with limbic encephalitis presenting with cognitive impairment and seizures. Recently, VGKC-complex antibodies have been described in a few children with limbic encephalitis, and children with unexplained encephalitis presenting with status epilepticus. We report a ca...

Journal: :Pediatric Neurology Briefs 2013

2016
Anna Marcé-Grau James Dalton Javier López-Pisón María Concepción García-Jiménez Lorena Monge-Galindo Ester Cuenca-León Jesús Giraldo Alfons Macaya

BACKGROUND De novo heterozygous mutations in the GNAO1 gene, encoding the Gα o subunit of G-proteins, are the cause of a severe neurodevelopmental disorder, featuring early infantile seizures, profound cognitive dysfunction and, occasionally, movement disorder (early infantile epileptic encephalopathy-17). METHODS We report a further case of this association in a 20 month-old Spanish girl wit...

Journal: :European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2010
Roberta Bombardieri Mariangela Pinci Romina Moavero Caterina Cerminara Paolo Curatolo

Epilepsy associated with tuberous sclerosis complex (TSC) is characterized by early onset and intractable seizures in the majority of children. There is a solid evidence of clinical efficacy of vigabatrin in interrupting infantile spasms associated with TSC. Due to an early diagnosis we were able to start vigabatrin at the very early onset of seizures in 10 children, who subsequently underwent ...

Journal: :The Journal of clinical investigation 2015
Christopher Patzke Yan Han Jason Covy Fei Yi Stephan Maxeiner Marius Wernig Thomas C Südhof

Heterozygous mutations in the syntaxin-binding protein 1 (STXBP1) gene, which encodes Munc18-1, a core component of the presynaptic membrane-fusion machinery, cause infantile early epileptic encephalopathy (Ohtahara syndrome), but it is unclear how a partial loss of Munc18-1 produces this severe clinical presentation. Here, we generated human ES cells designed to conditionally express heterozyg...

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