Headache as a sole manifestation in nonconvulsive status epilepticus.

Abstract:

:Nonconvulsive status epilepticus may present with several manifestations, and many of them may not be obvious. The most important for the diagnosis of nonconvulsive status epilepticus is the electroencephalogram pattern. This is a case report of a 9-year-old boy with severe and continuous headache. He received chemotherapy for histiocytosis that was diagnosed when he was 3 years, 6 months years old. He had no evidence of central nervous system histiocytosis involvement or drug toxicity. He was diagnosed with nonconvulsive status epilepticus. The headache and electroencephalogram anomaly disappeared completely when anticonvulsant therapy began. Headache and seizure disorder may coexist, but this may be the first report of nonconvulsive status epilepticus with headache as a sole manifestation.

journal_name

J Child Neurol

authors

Ghofrani M,Mahvelati F,Tonekaboni H

doi

10.1177/0883073807303252

subject

Has Abstract

pub_date

2007-05-01 00:00:00

pages

660-2

issue

5

eissn

0883-0738

issn

1708-8283

pii

22/5/660

journal_volume

22

pub_type

杂志文章
  • Pediatric acute transverse myelitis overview and differential diagnosis.

    abstract::Acute transverse myelitis is a clinical syndrome affecting the spinal cord, which is characterized by acute onset of motor, sensory, and autonomic dysfunction. Approximately 20% of cases of acute transverse myelitis occur in children. This review summarizes the current published literature on acute transverse myelitis...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073812452916

    authors: Wolf VL,Lupo PJ,Lotze TE

    更新日期:2012-11-01 00:00:00

  • Outpatient Procedural Sedation of Patients With Autism Spectrum Disorders for Magnetic Resonance Imaging of the Brain Using Propofol.

    abstract:OBJECTIVE:To quantify the number of personnel, time to induce and complete sedation using propofol for outpatient magnetic resonance imaging (MRI) of the brain, and the frequency of serious adverse events (SAEs) in children with autism spectrum disorder (ASD) compared with children without ASD. RESULTS:Baseline charac...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073817753908

    authors: Kamat PP,Karaga MK,Wisniewski BL,McCracken CE,Simon HK,Sidhu R,Grunwell JR

    更新日期:2018-04-01 00:00:00

  • Ten Years' Follow-Up of a Family With Myokymia and Muscle Cramps Without Ataxia.

    abstract::We report 10 years' follow-up of the previously described family with a novel mutation of the KCNA1 gene. The family consisted of 3 affected boys (first seen at ages 3, 11, and 12) and their affected mother and asymptomatic father and sister. They clinically presented with diffuse myokymia, muscle cramps, and lower li...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073812457461

    authors: Moghimi N,Rosen JB,Jabbari B

    更新日期:2013-11-01 00:00:00

  • Infantile Sandhoff's disease: multivoxel magnetic resonance spectrosecopy findings.

    abstract::Sandhoff's disease is a rare, genetic lysosomal storage disease leading to delayed myelination or demyelination. Although neuroimaging findings in this disease have been reported previously, magnetic resonance spectroscopy findings have not been reported. In this report, we present magnetic resonance imaging and magne...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738030180061201

    authors: Alkan A,Kutlu R,Yakinci C,Sigirci A,Aslan M,Sarac K

    更新日期:2003-06-01 00:00:00

  • Ocular motor behavior of children with neurofibromatosis 1.

    abstract::Patients with neurofibromatosis 1 show neurocognitive deficits including abnormal visuospatial performance, but oculomotor behavior has not been studied. We recorded saccades in neurofibromatosis 1 and normal children, ages 6 to 12 years. Patients showed increased latency and diminished amplitude to more eccentric tar...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738030180050301

    authors: Lasker AG,Denckla MB,Zee DS

    更新日期:2003-05-01 00:00:00

  • Electroretinographic responses in epileptic children treated with vigabatrin.

    abstract::Vigabatrin is an antiepileptic drug that results in higher gamma-aminobutyrate levels in the brain and retina. Vigabatrin-induced visual field defects are usually asymptomatic and only detectable by perimetry. Further, perimetry requires good cooperation, and children aged under 10 years cannot do it. Electroretinogra...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813490073

    authors: Bakhshandeh Bali MK,Otaghsara SM,Soltansanjari M,Sadighi N,Nasehi MM,Ashrafi MR,Karimzadeh P,Taghdiri MM,Ghofrani M

    更新日期:2014-06-01 00:00:00

  • Guidelines for resuscitation in the delivery room of extremely preterm infants.

    abstract::Ethical problems related to intensive care of extremely preterm newborns of < or = 25 weeks' gestational age and at risk of disability have been extensively debated. The Bioethical Committee of the Department of Paediatrics of the University Hospital of Padua organized and started a multidisciplinary group to release ...

    journal_title:Journal of child neurology

    pub_type: 指南,杂志文章,实务指引

    doi:10.1177/088307380401900106011

    authors: Verlato G,Gobber D,Drago D,Chiandetti L,Drigo P,Working Group of Intensive Care in the Delivery Room of Extremely Premature Newborns.

    更新日期:2004-01-01 00:00:00

  • Animal models of germinal matrix hemorrhage.

    abstract::Germinal matrix hemorrhage refers to bleeding that arises from the subependymal (or periventricular) germinal region of the immature brain. Clinical studies have shown that infants who experience germinal matrix hemorrhage can develop hydrocephalus or suffer from long-term neurologic dysfunction, including cerebral pa...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738060210050201

    authors: Balasubramaniam J,Del Bigio MR

    更新日期:2006-05-01 00:00:00

  • Pial Synangiosis Ameliorates Movement Disorders in the Absence of Prior Stroke in Moyamoya Disease.

    abstract:BACKGROUND:Moyamoya disease is a rare cerebrovascular disease characterized by progressive stenosis of the bilateral distal internal carotid arteries and their proximal branches. Both chorea and dystonia have been reported as the initial presentation of moyamoya disease. OBJECTIVE:The objective was to define the clini...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073815609152

    authors: Greene S,Bansal L,Coffman KA,Nardone R,Zuccoli G

    更新日期:2016-04-01 00:00:00

  • Impaired social behavior in children with benign childhood epilepsy with centrotemporal spikes.

    abstract::The aim of the present study was to assess the emotional and cognitive aspects of social cognition among patients with rolandic epilepsy. A computerized neuropsychological battery was used for cognitive evaluation. Affective and cognitive social cognition were evaluated using two computerized Theory of Mind tasks. Cog...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811414420

    authors: Genizi J,Shamay-Tsoory SG,Shahar E,Yaniv S,Aharon-Perez J

    更新日期:2012-02-01 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

  • The Most Common Comorbidities in Dandy-Walker Syndrome Patients: A Systematic Review of Case Reports.

    abstract:OBJECTIVE:Dandy-Walker syndrome (DWS) is a rare neurologic multi-entity malformation. This review aimed at reporting its main nonneurologic comorbidities. METHODS:Following PRISMA guidelines, search in Medline was conducted (2000-2014, keyword: dandy-walker). Age, sex, country, DWS type, consanguinity or siblings with...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073817712589

    authors: Stambolliu E,Ioakeim-Ioannidou M,Kontokostas K,Dakoutrou M,Kousoulis AA

    更新日期:2017-09-01 00:00:00

  • History of Joubert syndrome and a 30-year follow-up of the original proband.

    abstract::The 1960s were a period of great flowering in the recognition of neurologic disorders in children. The so-called ataxic cerebral palsies were an especially fertile field waiting for clarification. Congenital ataxia coupled with hyperpnea-apnea, abnormal eye movements, and retardation was identified as an autosomal-rec...

    journal_title:Journal of child neurology

    pub_type: 历史文章,杂志文章

    doi:10.1177/088307389901400903

    authors: Andermann F,Andermann E,Ptito A,Fontaine S,Joubert M

    更新日期:1999-09-01 00:00:00

  • Secondary erythromelalgia successfully treated with intravenous immunoglobulin.

    abstract::Erythromelalgia is a rare condition characterized by episodic painful erythema and warmth often affecting, but not limited to, the distal extremities. This condition is notoriously difficult to treat. We report a young female patient with seronegative polyarthritis who presented with a 6-year history of recurrent bout...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811427784

    authors: Moody S,Pacheco S,Butler IJ,Koenig MK

    更新日期:2012-07-01 00:00:00

  • Psychologic and neurologic function following treatment for childhood temporal lobe astrocytoma.

    abstract::Seven school-aged children treated for temporal lobe astrocytomas with surgical resection and irradiation were prospectively tested to evaluate their intellectual, academic, personality, and neurologic status after therapy. At their most recent follow-up examination, neuropsychologic functioning was adequate in only t...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388800300111

    authors: Mulhern RK,Kovnar EH,Kun LE,Crisco JJ,Williams JM

    更新日期:1988-01-01 00:00:00

  • A Proof-of-Principle, Case-Control Study to Compensate for Potential Carbohydrates in Liquid Antiseizure Drugs in Children on the Ketogenic Diet.

    abstract:INTRODUCTION:Since its creation, patients on ketogenic diet are told to avoid liquid medications due to theoretical concerns of "hidden" carbohydrates. However, switching from liquid to tablet formulations can be problematic, especially for infants and young children. We theorized that increasing the daily ketogenic ra...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073819831179

    authors: Haney CA,Charpentier A,Turner Z,Bessone SK,Doerrer SC,Kossoff EH

    更新日期:2019-06-01 00:00:00

  • Atypical teratoid/rhabdoid tumor of the spine in a 4-year-old girl.

    abstract::Primary spinal atypical teratoid/rhabdoid tumor is extremely rare. The authors present a case of atypical teratoid/rhabdoid tumor occurring in a 4-year-old girl. Magnetic resonance imaging The authors showed an intramedullary mass extending from the bulbomedullary junction to T1 with leptomeningeal dissemination. The ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808319319

    authors: Tinsa F,Jallouli M,Douira W,Boubaker A,Kchir N,Hassine DB,Boussetta K,Bousnina S

    更新日期:2008-12-01 00:00:00

  • Early-Onset Mild Type Leukoencephalopathy Caused by a Homozygous EARS2 Mutation.

    abstract::Childhood leukoencephalopathies are a broad class of diseases, which are extremely rare. The treatment and classification of these disorders are both challenging. Nearly half of children presenting with a leukoencephalopathy remain without a specific diagnosis. Leukoencephalopathy with thalamus and brain stem involvem...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073816630087

    authors: Taskin BD,Karalok ZS,Gurkas E,Aydin K,Aydogmus U,Ceylaner S,Karaer K,Yilmaz C,Pearl PL

    更新日期:2016-06-01 00:00:00

  • Pediatric-Onset Postural Orthostatic Tachycardia Syndrome in a Single Tertiary Care Center.

    abstract:AIM:We characterize the pediatric postural orthostatic tachycardia syndrome (POTS) population seen at a single tertiary care referral center. METHOD:Retrospective chart review of all pediatric POTS patients seen in our center between 2015 and 2017. Pediatric POTS was defined as chronic, at least 3 months, symptoms of ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820916260

    authors: Staples A,Thompson NR,Moodley M

    更新日期:2020-07-01 00:00:00

  • A case of giant intracranial tuberculoma in an infant: clinical and radiologic pitfalls.

    abstract::Intracranial tuberculoma in infants are a rare occurrence. We report a 7-month-old male infant presenting to our tertiary care referral center with complaints of global developmental delay and right hemiparesis for 3 months. Radiologic imaging was suggestive of large left frontoinsular space-occupying lesion with init...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814535487

    authors: Raheja A,Sinha S,Sable MN,Sharma MC,Sharma BS

    更新日期:2015-03-01 00:00:00

  • Meningismus is a commonly overlooked finding in tension-type headache in children and adolescents.

    abstract::At present, both migraine and tension-type headaches in children are believed to be chronic primary headaches. Meningeal signs in both cases are ignored or not examined, and the neurologic status is considered normal. This is the first study that focuses on meningeal signs in children with chronic headaches. The study...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738060210050601

    authors: Almazov I,Brand N

    更新日期:2006-05-01 00:00:00

  • Infant-onset progressive myoclonus epilepsy.

    abstract::We report the clinical, electroencephalographic, neurophysiologic, and neuroimaging findings in eight children with infant-onset progressive myoclonus epilepsy, all of whom had muscle biopsies performed as as part of the diagnostic evaluation. Each child had myoclonic seizures, generalized tonic-clonic seizures, and n...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389100600207

    authors: Harbord MG,Hwang PA,Robinson BH,Becker LE,Hunjan A,Murphy EG

    更新日期:1991-04-01 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

  • Classification of infantile seizures: implications for identification and treatment of inborn errors of metabolism.

    abstract::Metabolic disorders constitute an important cause of neurologic disease, including infantile epilepsy. The inability to characterize seizures and epilepsy syndromes precisely in infants impedes the recognition of features suggestive of specific underlying metabolic and neurodegenerative etiologies. Classification syst...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:

    authors: Nordli DR Jr,De Vivo DC

    更新日期:2002-12-01 00:00:00

  • Systemic and ocular findings in 100 patients with optic nerve hypoplasia.

    abstract::To describe associated ocular, neurologic, and systemic findings in a population of children with optic nerve hypoplasia, a retrospective chart review of 100 patients with optic nerve hypoplasia for the presence of neurologic, radiologic, and endocrine abnormalities was performed. Neuroimaging and endocrine studies we...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738060210111701

    authors: Garcia ML,Ty EB,Taban M,David Rothner A,Rogers D,Traboulsi EI

    更新日期:2006-11-01 00:00:00

  • Epilepsy and electroencephalographic findings in pericentric inversion of chromosome 12.

    abstract::Epilepsy, together with mental retardation, represents a common manifestation of chromosomal aberrations. Specific electroencephalographic (EEG) and epileptic patterns have been described in several chromosomal disorders, such as Angelman's syndrome, Miller-Dieker syndrome, Wolf-Hirschhorn syndrome, and ring 20 syndro...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380401900807

    authors: Grosso S,Pucci L,Farnetani M,Di Bartolo RM,Galimberti D,Mostardini R,Anichini C,Balestri M,Morgese G,Balestri P

    更新日期:2004-08-01 00:00:00

  • Can we identify predictors of multilevel botulinum toxin A injections in children with cerebral palsy who walk with a flexed knee pattern?

    abstract:UNLABELLED:This study evaluates whether the literature-reported potential predictors can predict the outcome of multilevel botulinum toxin A injections in children who walk with flexed knees. The associations between 11 different predictors and 2 different outcome measures (the Gross Motor Function Measure and knee ang...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究,随机对照试验

    doi:10.1177/0883073807313039

    authors: Scholtes VA,Dallmeijer AJ,Becher JG

    更新日期:2008-06-01 00:00:00

  • Brain tumors presenting as a seizure disorder in infants.

    abstract::Seizures occur in 25% to 40% of children with supratentorial tumors and are the presenting complaint in 10% to 15%. However, when divided by age, only 2% of children with seizures as the presenting complaint of brain tumors were less than 1 year of age. Three children, ranging in age from 20 days to 7 months and seen ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388700200308

    authors: Rutledge SL,Snead OC 3rd,Morawetz R,Chandra-Sekar B

    更新日期:1987-07-01 00:00:00

  • Study of nerve conduction and late responses in normal Chinese infants, children, and adults.

    abstract::Healthy Chinese individuals (n = 168), aged from 24 hours to 30 years, were studied to establish the following normal values: (1) motor conduction velocity, distal latency, amplitude, and F-wave velocity in the median, ulnar, tibial, and peroneal nerves; (2) H-reflex velocity and latency in the tibial nerve for all su...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389701200102

    authors: Cai F,Zhang J

    更新日期:1997-01-01 00:00:00

  • Diurnal Salivary Cortisol and Regression Status in MECP2 Duplication Syndrome.

    abstract::MECP2 duplication syndrome is an X-linked genomic disorder that is characterized by infantile hypotonia, intellectual disability, and recurrent respiratory infections. Regression affects a subset of individuals, and the etiology of regression has yet to be examined. In this study, alterations in the hypothalamus-pitui...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073815585577

    authors: Peters SU,Byiers BJ,Symons FJ

    更新日期:2016-02-01 00:00:00