نتایج جستجو برای: early infantile epileptic encephalopathy

تعداد نتایج: 725871  

2002
EERO LEINONEN

The existing theory of transient intermodulation distortion (TIM) is extended to cover the calculation of the duration of intermodulation bursts. It is shown that feedback values in excess of some 40 dB will cause large internal overshoots within the amplifier. The clipping of these overshoots due to the limited dynamic margins of the amplifier driver stages is shown to give rise to long period...

Journal: :Seizure 2012
Masao Adachi Yu Abe Yoko Aoki Yoichi Matsubara

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 mutat...

Journal: :Genetics and molecular research : GMR 2011
L Dong M Mao R Luo Y Tong D Yu

Infantile spasms are a severe epileptic encephalopathy with a variety of etiologies that occur in infancy and early childhood. Subjects with infantile spasms are at a higher risk for evolving into intractable epileptic spasms, tending to be refractory to conventional antiepileptic drugs. Genetic polymorphisms of the P-glycoprotein-encoding gene ABCB1 are suspected to be associated with pharmaco...

Journal: :Journal of child neurology 2012
Anastasia Gkampeta Evangelos Pavlou

West syndrome (infantile spasms) is an epileptic encephalopathy that includes psychomotor deterioration. In rare cases, it is due to an inherited, progressive metabolic disease. More than 25 inborn errors of metabolism have been considered etiologic or predisposing factors for infantile spasms. This is a review of the literature on reported cases of children diagnosed with a metabolic disease w...

2015
Anna Ka-Yee Kwong Alvin Chi-Chung Ho Cheuk-Wing Fung Virginia Chun-Nei Wong

Epileptic Encephalopathy (EE) is a heterogeneous condition in which cognitive, sensory and/or motor functions deteriorate as a consequence of epileptic activity, which consists of frequent seizures and/or major interictal paroxysmal activity. There are various causes of EE and they may occur at any age in early childhood. Genetic mutations have been identified to contribute to an increasing num...

Journal: :Seizure 1995
Sheila J. Wallace

The severe epilepsies of childhood are described briefly and information available on the efficacy of newly developed antiepileptic drugs (AEDs) in their control is reviewed. Therapeutic advances are awaited for early infantile epileptic encephalopathy, early myoclonic encephalopathy, progressive myoclonus epilepsies and Kojewnikow syndrome. West syndrome may respond to vigabatrin, and less pre...

2017
Lynette G. Sadleir Emily I. Mountier Deepak Gill Suzanne Davis Charuta Joshi Catherine DeVile Manju A. Kurian Simone Mandelstam Elaine Wirrell Katherine C. Nickels Hema R. Murali Gemma Carvill Candace T. Myers Heather C. Mefford Ingrid E. Scheffer

OBJECTIVE To define a distinct SCN1A developmental and epileptic encephalopathy with early onset, profound impairment, and movement disorder. METHODS A case series of 9 children were identified with a profound developmental and epileptic encephalopathy and SCN1A mutation. RESULTS We identified 9 children 3 to 12 years of age; 7 were male. Seizure onset was at 6 to 12 weeks with hemiclonic s...

2015
Tommy Stödberg Amy McTague Arnaud J Ruiz Hiromi Hirata Juan Zhen Philip Long Irene Farabella Esther Meyer Atsuo Kawahara Grace Vassallo Stavros M Stivaros Magnus K Bjursell Henrik Stranneheim Stephanie Tigerschiöld Bengt Persson Iftikhar Bangash Krishna Das Deborah Hughes Nicole Lesko Joakim Lundeberg Rod C Scott Annapurna Poduri Ingrid E Scheffer Holly Smith Paul Gissen Stephanie Schorge Maarten E A Reith Maya Topf Dimitri M Kullmann Robert J Harvey Anna Wedell Manju A Kurian

The potassium-chloride co-transporter KCC2, encoded by SLC12A5, plays a fundamental role in fast synaptic inhibition by maintaining a hyperpolarizing gradient for chloride ions. KCC2 dysfunction has been implicated in human epilepsy, but to date, no monogenic KCC2-related epilepsy disorders have been described. Here we show recessive loss-of-function SLC12A5 mutations in patients with a severe ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید