Childhood absence epilepsy: Elctroclinical features and diagnostic criteria.

Abstract:

OBJECTIVE:To analyze the electroclinical features of children with childhood absence epilepsy (CAE) and discuss the diagnostic criteria for CAE. METHODS:The video-electroencephalogram (VEEG) database in our hospital was searched using "absence seizures" and "3-Hz generalized spike and waves (GSW)" as key-words. Other epileptic syndromes with typical absence seizures were carefully excluded. Children meeting the CAE diagnostic criteria of the International League Against Epilepsy (ILAE) in 1989 were further evaluated with the diagnostic criteria proposed by Panayiotopoulos in 2005. RESULTS:Totally 37 children met the 1989 ILAE criteria of CAE. The onset age of absence seizures ranged from 3 to 11 years. All patients had frequent absence seizures (5-60 times per day). Two patients (5.4%) had generalized tonic-clonic seizures. Hyperventilation induced absences in all patients. VEEG confirmed that 7 patients (18.9%) had only simple absences, 25 patients (67.6%) had only complex absences, and 5 patients (13.5%) had both simple and complex absences. Ictal EEG showed 3Hz GSW discharges in all patients. The seizure duration ranged from 3 to 40s. Four patients (10.8%) had two spikes per wave in ictal EEG. GSW fragments were found in 29 patients (78.4%) during sleep. Interictal polyspikes and waves were present in 17 patients (45.9%). Focal discharges predominantly in the anterior regions, were found in 22 patients (56.8%). Only 7 patients (18.9%) met the diagnostic criteria proposed by Panayiotopoulos in 2005. CONCLUSIONS:Few patients meeting the 1989 ILAE diagnostic criteria for CAE meet the new diagnostic criteria proposed by Panayiotopoulos in 2005. The new criteria for CAE are too strict to appropriately classify some patients.

journal_name

Brain Dev

journal_title

Brain & development

authors

Ma X,Zhang Y,Yang Z,Liu X,Sun H,Qin J,Wu X,Liang J

doi

10.1016/j.braindev.2010.02.004

subject

Has Abstract

pub_date

2011-02-01 00:00:00

pages

114-9

issue

2

eissn

0387-7604

issn

1872-7131

pii

S0387-7604(10)00059-8

journal_volume

33

pub_type

杂志文章
  • The neurological outcomes of cerebellar injury in premature infants.

    abstract:AIM:Cerebellar injury is a characteristic injury associated with preterm infants. However, the impact of cerebellar injury on the development of preterm infants is unclear. METHOD:We reviewed magnetic resonance image studies of preterm infants with cerebral palsy retrospectively and evaluated the developmental outcome...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2015.01.009

    authors: Kobayashi S,Wakusawa K,Inui T,Tanaka S,Kobayashi Y,Onuma A,Haginoya K

    更新日期:2015-10-01 00:00:00

  • Non-invasive screening of fragile X syndrome A using urine and hair roots.

    abstract::The diagnosis of fragile X A syndrome (FRAXA) during childhood depends largely on DNA-based diagnostic tests due to the lack of the specific clinical features. To determine a non-invasive screening method for fragile X syndrome, we studied the method of DNA-based diagnosis using urine or hair roots instead of routinel...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2003.11.002

    authors: Suwa K,Momoi MY

    更新日期:2004-09-01 00:00:00

  • Neuroprotective effect of human placental extract on hypoxic-ischemic brain injury in neonatal rats.

    abstract::We investigated the neuroprotective effects of human placental extracts (HPE) and the effects of HPE on recovery of cognitive and behavioral function on hypoxic-ischemic brain injury in the newborn rat. The right common carotid arteries of 7-day-old rats were coagulated, and rats were then exposed to 8% oxygen. Immedi...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2012.01.009

    authors: Park JY,Byeon JH,Park SW,Eun SH,Chae KY,Eun BL

    更新日期:2013-01-01 00:00:00

  • Developmental expression of monocyte chemoattractant protein-1 in the human cerebellum and brainstem.

    abstract::The developmental expression of monocyte chemoattractant protein-1 (MCP-1) in the cerebellum, medulla oblongata and pons was investigated in 26 normal human brains, ranging from 20 weeks of gestation (GW) to adulthood by means of an immunohistochemical method. Immunoreactivity to MCP-1 was observed in neurons of the c...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(98)00065-5

    authors: Meng SZ,Oka A,Takashima S

    更新日期:1999-01-01 00:00:00

  • Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene.

    abstract::Choline kinase beta gene (CHKB) mutations have been identified in Megaconial Congenital Muscular Dystrophy (MDCMC) patients, a very rare inborn error of metabolism with 21 cases reported worldwide. We report the case of a Spanish boy of Caucasian origin who presented a generalized congenital muscular hypotonia, more i...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2015.05.008

    authors: Castro-Gago M,Dacruz-Alvarez D,Pintos-Martínez E,Beiras-Iglesias A,Arenas J,Martín MÁ,Martínez-Azorín F

    更新日期:2016-01-01 00:00:00

  • Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome.

    abstract::Mutations of the gene encoding the alpha2 subunit of the neuronal sodium channel, SCN2A, have been found in benign familial neonatal-infantile seizures (BFNIS). In Dravet syndrome, only one nonsense mutation of SCN2A was identified, while hundreds of mutations were found in the paralogue gene, SCN1A, which encodes the...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2009.08.009

    authors: Shi X,Yasumoto S,Nakagawa E,Fukasawa T,Uchiya S,Hirose S

    更新日期:2009-11-01 00:00:00

  • Clinical and MRI findings in a case of D-2-hydroxyglutaric aciduria.

    abstract::We report the 3rd case in the literature of a 3-year-old boy with D-2-hydroxyglutaric (D-2-HG) aciduria, who presented primarily generalized hypotonia and feeding difficulty during the neonatal period, with eventual development of generalized myoclonic seizures. Gas chromatographic analysis of urinary organic acids sh...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/0387-7604(94)00123-f

    authors: Sugita K,Kakinuma H,Okajima Y,Ogawa A,Watanabe H,Niimi H

    更新日期:1995-03-01 00:00:00

  • Pharmacokinetics of zonisamide in perinatal period.

    abstract::Zonisamide is widely used for intractable epilepsy and the effects of this drug on fetuses and neonates through the mother taking it for epilepsy need to be clarified. We measured the zonisamide concentration in plasma and breast milk using high-performance liquid chromatography to investigate the transfer of zonisami...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(01)00407-7

    authors: Kawada K,Itoh S,Kusaka T,Isobe K,Ishii M

    更新日期:2002-03-01 00:00:00

  • Vitamin B6 in acute encephalopathy with biphasic seizures and late reduced diffusion.

    abstract:BACKGROUND:The initial presentation of acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is indistinguishable from that of complex febrile seizures (FS), which poses a great diagnostic challenge for clinicians. Excitotoxicity is speculated to be the pathogenesis of AESD. Vitamin B6 (VB6) is ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2020.02.002

    authors: Akiyama T,Toda S,Kimura N,Mogami Y,Hanaoka Y,Tokorodani C,Ito T,Miyahara H,Hyodo Y,Kobayashi K

    更新日期:2020-05-01 00:00:00

  • Isolated pyramidal tract impairment in the central nervous system of adult-onset Krabbe disease with novel mutations in the GALC gene.

    abstract::This report describes a 60-year-old female patient with Krabbe disease who presented with slowly progressive gait disturbance due to mild spastic paraplegia. Brain magnetic resonance imaging showed high-intensity lesions along the upper parts of the bilateral pyramidal tracts in fluid-attenuated inversion recovery ima...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2012.08.004

    authors: Tokushige S,Sonoo T,Maekawa R,Shirota Y,Hanajima R,Terao Y,Matsumoto H,Hossain MA,Sakai N,Shiio Y

    更新日期:2013-06-01 00:00:00

  • Infantile hypophosphatasia combined with vitamin B6-responsive seizures and reticular formation lesions on magnetic resonance imaging: A case report.

    abstract:BACKGROUND:Hypophosphatasia (HPP) is a rare genetic disorder characterized by rachitic bone manifestations and a low serum alkaline phosphatase (ALP) level. It is caused by mutations in the tissue non-specific alkaline phosphatase (TNSALP) gene, which encodes the tissue non-specific isozyme of ALP. HPP patients exhibit...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2017.07.015

    authors: Fukazawa M,Tezuka J,Sasazuki M,Masumoto N,Baba H,Doi T,Tsutsumi Y,Mizuno Y,Mihara F,Nakayama H

    更新日期:2018-02-01 00:00:00

  • Immunological aspects of epilepsy.

    abstract::Approximately 10% of patients with systemic lupus erythematosus (SLE) develop epileptic seizures. When occurring before the onset of generalized SLE, the seizures are mainly primary generalized. Accordingly, long-term treatment with anti-epileptic drugs may precipitate SLE, or epilepsy and SLE may both occur as manife...

    journal_title:Brain & development

    pub_type: 杂志文章,评审

    doi:10.1016/0387-7604(93)90005-s

    authors: Aarli JA

    更新日期:1993-01-01 00:00:00

  • De novo HDAC8 mutation causes Rett-related disorder with distinctive facial features and multiple congenital anomalies.

    abstract::We present a unique 11-year-old girl showing clinical features of Rett-related disorder with distinctive facial features and multiple congenital anomalies including ocular hypertelorism, arched eyebrows, a broad nose, dental anomalies, congenital heart disease, truncal obesity, and epilepsy. A novel de novo mutation i...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2017.12.013

    authors: Saikusa T,Hara M,Iwama K,Yuge K,Ohba C,Okada JI,Hisano T,Yamashita Y,Okamoto N,Saitsu H,Matsumoto N,Matsuishi T

    更新日期:2018-05-01 00:00:00

  • Extremely preterm infants small for gestational age are at risk for motor impairment at 3 years corrected age.

    abstract:BACKGROUND:Few studies have targeted psychomotor development and associated perinatal risk factors in Japanese very low birth weight (VLBW) infants who are severely small for gestational age (SGA). DESIGN/SUBJECTS:A single-center study was conducted in 104 Japanese VLBW infants who were born preterm, due to maternal, ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2015.07.008

    authors: Kato T,Mandai T,Iwatani S,Koda T,Nagasaka M,Fujita K,Kurokawa D,Yamana K,Nishida K,Taniguchi-Ikeda M,Tanimura K,Deguchi M,Yamada H,Iijima K,Morioka I

    更新日期:2016-02-01 00:00:00

  • Fibroblast screening for chaperone therapy in beta-galactosidosis.

    abstract::We performed screening of beta-galactosidase-deficient fibroblasts for possible chemical chaperone therapy using N-octyl-4-epi-beta-valienamine (NOEV) in patients with GM1-gangliosidosis and Morquio B disease (beta-galactosidosis). Fibroblasts were cultured with NOEV for 4 days and beta-galactosidase activity was meas...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2006.02.002

    authors: Iwasaki H,Watanabe H,Iida M,Ogawa S,Tabe M,Higaki K,Nanba E,Suzuki Y

    更新日期:2006-09-01 00:00:00

  • Magnetic resonance studies of brain lesions in patients with Kawasaki disease.

    abstract::We evaluated brain lesions in patients with coronary arterial lesions (CAL) as a complication of Kawasaki disease (KD) by magnetic resonance imaging (MRI) and magnetic resonance angiography (MRA). Among 47 patients who underwent coronary angiography for the evaluation of CAL due to KD at Kyushu University Hospital fro...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2005.04.003

    authors: Muneuchi J,Kusuhara K,Kanaya Y,Ohno T,Furuno K,Kira R,Mihara F,Hara T

    更新日期:2006-01-01 00:00:00

  • Inappropriate intracranial hemodynamics in the natural course of MELAS.

    abstract::The abnormalities of intracranial hemodynamics associated with strokelike episodes in MELAS are variable depend on the time phase from the onset of strokelike episodes and on the progression of the dementia state. To clarify the regional cerebral blood flows (rCBF) in the natural course of MELAS is very important to u...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2007.06.008

    authors: Nishioka J,Akita Y,Yatsuga S,Katayama K,Matsuishi T,Ishibashi M,Koga Y

    更新日期:2008-02-01 00:00:00

  • Bickerstaff's brainstem encephalitis with overlapping Guillain-Barré syndrome: Usefulness of sequential nerve conduction studies.

    abstract::Bickerstaff's brainstem encephalitis (BBE) is a rare immune-mediated disorder characterized by ophthalmoplegia, ataxia and disturbance of consciousness, which may overlap with Guillain-Barré syndrome (GBS) if there is additional limb weakness. We report a 7-month-old boy presented with ophthalmoplegia followed by a ra...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2018.02.001

    authors: Fong CY,Aung HWW,Khairani A,Gan CS,Shahrizaila N,Goh KJ

    更新日期:2018-06-01 00:00:00

  • Breathing disorders in males with acquired encephalopathy.

    abstract::Six boys affected by acquired encephalopathy with an abnormal breathing pattern in wakefulness were studied. Polygraphic recordings showed two different patterns in our population. In two brothers a periodic breathing pattern was recorded in the awake and sleep states. In the others, central apneas with or without tac...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(12)80180-x

    authors: Cirignotta F,Sforza E,Burroni M,Zappella M,Lugaresi E

    更新日期:1990-01-01 00:00:00

  • Risk factors for recurrence after drug withdrawal in childhood epilepsy.

    abstract:BACKGROUND:Several studies have been conducted to determine the risk of recurrence after withdrawal of antiepileptic drugs (AEDs) in recent years. There is no consensus concerning the circumstances affecting discontinuation of AEDs. This study was designed to determine the recurrence rate of epilepsy after withdrawal o...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2019.08.012

    authors: Karalok ZS,Guven A,Öztürk Z,Gurkas E

    更新日期:2020-01-01 00:00:00

  • Antiepileptic effects of clobazam in children.

    abstract::Many benzodiazepines used as anticonvulsants have nitrogen radicals in positions 1 and 4. Clobazam has nitrogen radicals in positions 1 and 5. We studied the antiepileptic effect of clobazam in 36 patients with intractable epilepsies in childhood. Their ages were 1 year 1 month to 16 years 5 months (mean 8 years). The...

    journal_title:Brain & development

    pub_type: 临床试验,杂志文章

    doi:10.1016/s0387-7604(82)80102-2

    authors: Shimizu H,Abe J,Futagi Y,Onoe S,Tagawa T,Mimaki T,Yamatodani A,Kato M,Kamio M,Sumi K,Sugita T,Yabuuchi H

    更新日期:1982-01-01 00:00:00

  • Posterior fossa cystic lesions--magnetic resonance imaging manifestations.

    abstract::Cystic lesions of the posterior fossa remain a controversial subject as to clinical classification and diagnosis, especially for those in combination with other intracranial abnormalities. During the period of November 1985 to June 1991, 16 patients with cystic lesions of the posterior fossa were retrospectively revie...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/0387-7604(95)00067-4

    authors: Tan EC,Takagi T,Karasawa K

    更新日期:1995-11-01 00:00:00

  • A case of hypertensive encephalopathy with extensive spinal lesions on MRI.

    abstract::A 14-year-old female had repeated vomiting, headache, abdominal pain, visual field deficit and lethargy at the onset of hypertensive encephalopathy. Cerebrospinal fluid (CSF) test revealed a high level of IgG and protein. MRI demonstrated no supratentorial cerebral lesions but hyperintense lesions were observed from t...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2009.07.002

    authors: Nagato M,Takahashi Y,Yoshioka M,Nambu M

    更新日期:2010-08-01 00:00:00

  • Sleep cyclic alternating pattern analysis in healthy children during the first year of life: a daytime polysomnographic study.

    abstract::We evaluated the cyclic alternating pattern (CAP) during the first year of life in order to obtain information on the maturation of arousal mechanisms during NREM sleep and to provide normative data for CAP parameters in this age range (5-16months). Eleven healthy children (mean age 7.9±3.3months, seven boys) were stu...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2010.07.008

    authors: Miano S,Peraita-Adrados R,Montesano M,Castaldo R,Forlani M,Villa MP

    更新日期:2011-05-01 00:00:00

  • Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes.

    abstract::A research committee supported by the Japanese government conducted a nationwide survey on the epidemiology of acute encephalopathy in Japan using a questionnaire. A total of 983 cases reportedly had acute encephalopathy during the past 3 years, 2007-2010. Among the pathogens of the preceding infection, influenza viru...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2011.07.012

    authors: Hoshino A,Saitoh M,Oka A,Okumura A,Kubota M,Saito Y,Takanashi J,Hirose S,Yamagata T,Yamanouchi H,Mizuguchi M

    更新日期:2012-05-01 00:00:00

  • Long-term prognosis of patients with West syndrome in Japan: social aspects.

    abstract::Long-term social prognosis of 120 Japanese patients with West syndrome was surveyed using structured questionnaire at the age of 25.4 years in average. The survey revealed that ADL score remained null in one-fifth of cases; the majority entered in special education course for disabled children; only eleven cases were ...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(01)00269-8

    authors: Kumagai T,Ito M,Yamazaki Y,Sekijima K,Sakakibara K,Matsutomo Y,Hijikigawa F,Yamada H

    更新日期:2001-11-01 00:00:00

  • Post-traumatic syndrome after minor head injury cannot be predicted by neurological investigations.

    abstract::The aim of this study is to investigate predictive factors of post-traumatic syndrome in children with minor head injury. Prospective neurological, electroencephalographic and psychological investigations were performed in 98 children aged 3-13 years within 24 h after the trauma and 4-6 weeks later. Inclusion criteria...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/S0387-7604(03)00110-4

    authors: Korinthenberg R,Schreck J,Weser J,Lehmkuhl G

    更新日期:2004-03-01 00:00:00

  • Influence of ACTH therapy on overnight sleep polygrams in infantile spasms.

    abstract::Overnight sleep polygrams were recorded before and during therapy in nine patients with infantile spasms. Results showed that ACTH therapy increased the waking time and decreased rapid eye movement sleep. Thus it caused sleep disturbance in patients with infantile spasms. During ACTH therapy the number of rapid eye mo...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/s0387-7604(81)80006-x

    authors: Hashimoto T,Hiura K,Suzue J,Nokawa T,Fukuda K,Endo S,Tayama M,Tamura Y,Miyao M

    更新日期:1981-01-01 00:00:00

  • Eye contact and emotional face processing in 6-month-old infants: advanced statistical methods applied to event-related potentials.

    abstract::Event-related potential (ERP) studies with infants are often limited by a small number of measurements. We introduce a weighted general linear mixed model analysis with a time-varying covariate, which allows for the efficient analysis of all available event-related potential data of infants. This method allows control...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2009.04.001

    authors: Stahl D,Parise E,Hoehl S,Striano T

    更新日期:2010-04-01 00:00:00

  • Childhood-onset anti-MuSK antibody positive myasthenia gravis demonstrates a distinct clinical course.

    abstract::Anti-muscle-specific tyrosine kinase antibody (MuSK-Ab) is the second most frequent autoantibody identified in adult patients with myasthenia gravis (MG). Adult patients with MuSK-Ab demonstrate characteristic clinical features but very little information is available for childhood-onset patients with MuSK-positive MG...

    journal_title:Brain & development

    pub_type: 杂志文章

    doi:10.1016/j.braindev.2011.12.014

    authors: Takahashi Y,Sugiyama M,Ueda Y,Itoh T,Yagyu K,Shiraishi H,Ukeba-Terashita Y,Nakanishi M,Nagashima T,Imai T,Motomura M,Saitoh S

    更新日期:2012-10-01 00:00:00