Epilepsy treatment in Rett syndrome.

Abstract:

:Rett syndrome is a neurodevelopmental disorder predominately affecting females. The majority of patients have epilepsy in the early stages of the disease. This study evaluates the clinical course of epilepsy and the effect of antiepileptic drug treatment in Rett syndrome using retrospective data analysis. Epilepsy was present in 16 of 19 (84%) patients with Rett syndrome in this series. The mean age of seizure onset was 4 years. Remission of seizures was achieved after the first monotherapy in 56% and after the second monotherapy in 18.5% of patients. Valproate, lamotrigine, and carbamazepine were the drugs used most frequently as monotherapy. Valproate monotherapy was highly effective as 75% of treated patients achieved seizure remission. Monotherapy with lamotrigine or carbamazepine was effective in half of the treated patients. There was a clear tendency toward seizure remission after the age of 15 years.

journal_name

J Child Neurol

authors

Krajnc N,Župančič N,Oražem J

doi

10.1177/0883073811408422

subject

Has Abstract

pub_date

2011-11-01 00:00:00

pages

1429-33

issue

11

eissn

0883-0738

issn

1708-8283

pii

0883073811408422

journal_volume

26

pub_type

杂志文章
  • Developmental and behavior problems predict parenting stress in young children with global delay.

    abstract::To identify parent-reported symptoms that predict parenting stress in preschoolers with global developmental delay, 201 parents/guardians of 142 boys and 59 girls with global delay, mean age 39.1 months (range, 18 to 63 months) were studied retrospectively. Parents completed the following: (a) a semistructured intervi...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811418230

    authors: Tervo RC

    更新日期:2012-03-01 00:00:00

  • What is attention-deficit hyperactivity disorder (ADHD)?

    abstract::Attention-deficit hyperactivity disorder (ADHD) is described as the most common neurobehavioral condition of childhood. We raise the concern that ADHD is not a disease per se but rather a group of symptoms representing a final common behavioral pathway for a gamut of emotional, psychological, and/or learning problems....

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738050200121301

    authors: Furman L

    更新日期:2005-12-01 00:00:00

  • Interleukin-1alpha, interleukin-1beta, and interleukin-1Ra polymorphisms in febrile seizures.

    abstract::Febrile seizures are the most common form of childhood seizures. The exact mechanism promoting convulsions during a common febrile illness remains unknown, but it is accepted that genetic influences are likely to account for at least some of the cases. Previous studies reported high interleukin-1beta levels in the cer...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200070401

    authors: Haspolat S,Baysal Y,Duman O,Coşkun M,Tosun O,Yeğin O

    更新日期:2005-07-01 00:00:00

  • Asymmetries in brain maturation and behavioral disturbances: multivariate electroencephalogram and P300 studies.

    abstract::If behavior results from brain function, some evidence of dysfunction could be expected in children with major behavioral problems. Yet, neurophysiologic studies in these children are frequently normal. We hypothesized a relationship between maturational asymmetry and behavior, given the role of hemispheric imbalance ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389901400206

    authors: Gerez M,Tello A,Serrano C,Ibarra R,Mallet A

    更新日期:1999-02-01 00:00:00

  • Experimental Therapeutic Trial Design for Pediatric Brain Tumors.

    abstract::Pediatric brain tumors are the leading cause of cancer-related death during childhood. Since the first pediatric brain tumor clinical trials, the field has seen improved outcomes in some, but not all tumor types. In the past few decades, a number of promising new therapeutic agents have emerged, yet only a few of thes...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073815604221

    authors: Bornhorst M,Hwang EI

    更新日期:2016-10-01 00:00:00

  • Genetic risk factors associated with thrombosis in children with congenital neurologic disorders.

    abstract::Thromboembolic events during the perinatal period are responsible for irreversible brain damage owing to cerebral hypoxia and neuronal necrosis. We investigated the presence of thrombophilia risk factors in children with congenital neurologic disorders. Nineteen children (9 males and 10 females), aged 1 to 14 years (m...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200060701

    authors: Tzoufi M,Giotopoulou S,Papadimitriou P,Dokou E,Kolaitis NI,Siamopoulou A,Vartholomatos G

    更新日期:2005-06-01 00:00:00

  • Comparative neuroimaging with pathologic correlates in Alexander's disease.

    abstract::We describe a case of pathologically confirmed Alexander's disease in which serial cranial ultrasound studies demonstrated unique findings of enlarging subependymal cysts with evolving periventricular hyperechogenicity. Computed tomographic scan of the head showed low attenuation of the periventricular white matter an...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389000500320

    authors: Hess DC,Fischer AQ,Yaghmai F,Figueroa R,Akamatsu Y

    更新日期:1990-07-01 00:00:00

  • Emergency Department Management of Pediatric Unprovoked Seizures and Status Epilepticus in the State of Illinois.

    abstract::The purpose of this survey and record review was to characterize emergency department management of unprovoked seizures and status epilepticus in children in Illinois. The survey was sent to 119 participating emergency departments in the Emergency Medical Services for Children program; responses were received from 103...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814566626

    authors: Taylor C,Piantino J,Hageman J,Lyons E,Janies K,Leonard D,Kelley K,Fuchs S

    更新日期:2015-10-01 00:00:00

  • Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)].

    abstract::Smith-Magenis syndrome is a multiple congenital anomalies/mental retardation syndrome associated with a heterozygous deletion of chromosome 17p11.2. Seizures have not been formally studied in this population. Our objectives were to estimate the prevalence of seizures and electroencephalographic (EEG) epileptiform abno...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738060210021201

    authors: Goldman AM,Potocki L,Walz K,Lynch JK,Glaze DG,Lupski JR,Noebels JL

    更新日期:2006-02-01 00:00:00

  • Early cognitive outcome after neonatal stroke.

    abstract::The purpose of this study was to assess the cognitive development of 27 children with nonhemorrhagic neonatal stroke (occurring within the first 28 days of life). The cognitive evaluation consisted of the Bayley Scales of Infant Development, administered at 12 and/or 24 months poststroke. Compared with the normative s...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073807305784

    authors: McLinden A,Baird AD,Westmacott R,Anderson PE,deVeber G

    更新日期:2007-09-01 00:00:00

  • Valuation of Quality of Life in Pediatric Disability in a Developing Country.

    abstract::This article assessed how Indian providers and mothers value quality of life in pediatric disabilities, hypothesizing lower values with increasing disability, lower values among providers than mothers, and lower values among mothers with versus mothers without a disabled child. We asked 175 participants: "If born tomo...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073818773941

    authors: Spiegel E,Jondhale S,Brajkovic I,Nesbit KC,Allen IE,Bhutani V,Kumar P,Partridge JC

    更新日期:2018-08-01 00:00:00

  • Initial management of childhood brain tumors: neurosurgical considerations.

    abstract::Intracranial tumors are the most common solid tumors in children. The infratentorial compartment will be the primary site for 60% to 70% of these tumors, including astrocytomas, medulloblastomas, and ependymomas. Several technological advancements have increased our knowledge of the cell biology of pediatric brain tum...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073808321768

    authors: Nejat F,El Khashab M,Rutka JT

    更新日期:2008-10-01 00:00:00

  • Proton magnetic resonance spectroscopy in a case of subacute sclerosing panencephalitis.

    abstract::Subacute sclerosing panencephalitis is an encephalopathy caused by a persistent measles virus infection. We examined a 13-year-old girl with subacute sclerosing panencephalitis and performed a magnetic resonance spectroscopic study to evaluate the in vivo pathophysiologic abnormality. The results suggested the occurre...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738020170101809

    authors: Kato Z,Saito K,Yamada M,Asano T,Kondo N

    更新日期:2002-10-01 00:00:00

  • Classification and natural history of the neuronal ceroid lipofuscinoses.

    abstract::The neuronal ceroid lipofuscinoses represent a group of disorders characterized by neurodegeneration and intracellular accumulation of an auto-fluorescent lipopigment (ceroid lipofuscin). Together, they represent the most prevalent class of childhood neurodegenerative disease. The neuronal ceroid lipofuscinoses encomp...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073813494268

    authors: Mink JW,Augustine EF,Adams HR,Marshall FJ,Kwon JM

    更新日期:2013-09-01 00:00:00

  • Corpus Callosotomy for Intractable Epilepsy Revisited: The Children's Hospital of Michigan Series.

    abstract::Corpus callosotomy is a palliative procedure performed to reduce the severity of drug-resistant epilepsy. The authors assessed its efficacy on different seizure types in 20 subjects (age range 5-19 years); 8 with active vagus nerve stimulator. Fifteen had complete callosotomy, 3 had anterior 2/3, and 2 had anterior 2/...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073817697847

    authors: Luat AF,Asano E,Kumar A,Chugani HT,Sood S

    更新日期:2017-06-01 00:00:00

  • Idiopathic photosensitive occipital epilepsy: clinical and electroencephalographic (EEG) features.

    abstract::Idiopathic photosensitive occipital lobe epilepsy is a reflex, age- and localization-related syndrome. We describe the clinical and electroencephalographic features, therapy, and outcome of 16 children/adolescents with this syndrome. The cohort included 2 sets of siblings and 7 patients with other first- or second-deg...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073812473366

    authors: Politi-Elishkevich K,Kivity S,Shuper A,Levine H,Goldberg-Stern H

    更新日期:2014-03-01 00:00:00

  • Endocrine disorders in two sisters affected by MELAS syndrome.

    abstract::A variety of endocrine and metabolic defects, including hypothalamopituitary hypofunction and diabetes mellitus, has been reported in association with mitochondrial disorders. We describe two sisters affected by mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome in whom DNA anal...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001501108

    authors: Balestri P,Grosso S

    更新日期:2000-11-01 00:00:00

  • Venlafaxine in children, adolescents, and young adults with autism spectrum disorders: an open retrospective clinical report.

    abstract::Autism is characterized by social deficits, communication and language impairments, narrow restricted interests, repetitive behaviors, inattention, and hyperactivity. While selective serotonin reuptake inhibitors have demonstrated efficacy in treating core symptoms of autism, norepinephrine reuptake inhibitors have de...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380001500214

    authors: Hollander E,Kaplan A,Cartwright C,Reichman D

    更新日期:2000-02-01 00:00:00

  • Electroencephalographic correlate of juvenile Huntington's disease.

    abstract::The spectrum of clinical disease in juvenile Huntington's disease differs from that seen in adults. Younger patients often present with seizures, dystonia and rigidity. The mechanism and type of seizures, timing of onset and electrographic features have not been well characterized in either adults or children. We desc...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:

    authors: Ullrich NJ,Riviello JJ Jr,Darras BT,Donner EJ

    更新日期:2004-07-01 00:00:00

  • A Novel Treatment Strategy for Severe Guillain-Barré Syndrome: Zipper Method.

    abstract:OBJECTIVE:Intravenous immunoglobulin and plasma exchange are proven treatments for Guillain-Barré syndrome. Despite these treatments, the prognosis for severe Guillain-Barré syndrome is still not satisfactory. This article seeks for a logical timing for plasma exchange-intravenous immunoglobulin synergy, which may impr...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073819826225

    authors: Kesici S,Tanyıldız M,Yetimakman F,Bayrakci B

    更新日期:2019-04-01 00:00:00

  • Postinfectious myasthenia gravis: report of two children.

    abstract::We report two children with transient myasthenia gravis preceded by viral illnesses. The first is a 5-year-old boy who developed oculobulbar weakness 2 weeks following a varicella-zoster infection. The second is a 4-year-old boy who developed facial diplegia and dysarthria several weeks following a viral pharyngitis. ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200051501

    authors: Felice KJ,DiMario FJ,Conway SR

    更新日期:2005-05-01 00:00:00

  • Recurrent acute necrotizing encephalopathy in a Korean child: the first non-Caucasian case.

    abstract::Acute necrotizing encephalopathy is characterized by fever, seizures, acute encephalopathy, and rapid progression to coma. It is usually associated with viral illness and shows characteristic brain magnetic resonance imaging features, including symmetrical involvement of bilateral thalami, brain stem, white matter, an...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811435240

    authors: Lee JH,Lee M,Lee J

    更新日期:2012-10-01 00:00:00

  • Neurodevelopmental outcome of severe neonatal hemolytic hyperbilirubinemia.

    abstract::We recruited 128 neonates with hyperbilirubinemia over a 5-year period (1995-2000) to study the short- and long-term effects of hemolytic hyperbilirubinemia on the auditory brainstem pathway and neurodevelopmental status. These children were divided into two groups: (1) a hemolytic group (n = 29; ABO incompatibility [...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738060210061301

    authors: Chen WX,Wong VC,Wong KY

    更新日期:2006-06-01 00:00:00

  • Vigabatrin in refractory epilepsy in adults and its application in children.

    abstract::Vigabatrin has been studied in adult drug-resistant epilepsy since 1982 in single-blind and double-blind studies followed by long-term, open evaluations. These studies have provided evidence that vigabatrin is a potent and well-tolerated antiepileptic drug and support its potential value in pediatric epilepsy. The lac...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:

    authors: Dam M

    更新日期:1991-01-01 00:00:00

  • Intrauterine endotoxin administration leads to white matter diffusivity changes in newborn rabbits.

    abstract::Maternal intrauterine inflammation has been implicated in the development of periventricular leukomalacia and white matter injury in the neonate. We hypothesized that intrauterine endotoxin administration would lead to microstructural changes in the neonatal rabbit white matter in vivo that could be detected at birth ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073809338213

    authors: Saadani-Makki F,Kannan S,Makki M,Muzik O,Janisse J,Romero R,Chugani D

    更新日期:2009-09-01 00:00:00

  • Cerebrospinal fluid neuron-specific enolase following seizures in children: role of etiology.

    abstract::Neuron-specific enolase, a marker for neuronal injury, is elevated following seizures in adults, but relatively few data exist on postictal neuron-specific enolase levels in children. This study measured cerebrospinal fluid (CSF) neuron-specific enolase levels after seizures in 49 consecutive pediatric patients and in...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700404

    authors: Wong M,Ess K,Landt M

    更新日期:2002-04-01 00:00:00

  • Factors predictive of outcome in childhood epilepsy.

    abstract::To identify early predictive factors of outcome in childhood epilepsy, the case records of all children with new-onset epilepsy presenting to a single neurology practice over a 10-year interval were reviewed. Only children with more than 2 years of follow-up were included. Cox regression analysis was used to identify ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738050200110701

    authors: Oskoui M,Webster RI,Zhang X,Shevell MI

    更新日期:2005-11-01 00:00:00

  • Intracranial tumors in infants.

    abstract::The prognosis in infants with brain tumors has historically been very poor. This study reviews 16 infants under the age of 12 months with brain tumors who presented to our institution between 1988 and 1999. The aim was to describe the clinical presentation, diagnosis, and management of these patients and to establish ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380401900605

    authors: Young HK,Johnston H

    更新日期:2004-06-01 00:00:00

  • Cerliponase Alfa for the Treatment of Atypical Phenotypes of CLN2 Disease: A Retrospective Case Series.

    abstract:BACKGROUND:The classic phenotype of CLN2 disease (neuronal ceroid lipofuscinosis type 2) typically manifests between ages 2 and 4 years with a predictable clinical course marked by epilepsy, language developmental delay, and rapid psychomotor decline. Atypical phenotypes exhibit variable time of onset, symptomatology, ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820977997

    authors: Wibbeler E,Wang R,Reyes EL,Specchio N,Gissen P,Guelbert N,Nickel M,Schwering C,Lehwald L,Trivisano M,Lee L,Amato G,Cohen-Pfeffer J,Shediac R,Leal-Pardinas F,Schulz A

    更新日期:2020-12-23 00:00:00

  • Current status of treatments for dyslexia: critical review.

    abstract::The acquisition of reading is a complex neurobiologic process. Identifying the most effective instruction and remedial intervention methods for children at risk of developing reading problems and for those who are already struggling is equally complex. This article aims to provide the clinician with a review of more c...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738040190100401

    authors: Alexander AW,Slinger-Constant AM

    更新日期:2004-10-01 00:00:00