Bilateral basal ganglia lesions after hypoglycemic coma in a 6-year-old child.

Abstract:

:Imaging findings of brain damage due to neonatal hypoglycemia are known; however, the effect of childhood hypoglycemia on the brain has not been described well. The authors present the case of a 6-year-old girl who had seizures secondary to hypoglycemia followed up for 1 year as epilepsy. The patient had experienced a hypoglycemic coma attack about 1 year before. Brain magnetic resonance imaging showed atrophy of the cerebrum and cerebellum and bilateral symmetrically hyperintense lesions in the putamina. The patient was diagnosed with hypoglycemia due to hyperinsulinism.

journal_name

J Child Neurol

authors

Kara C,Aydin OF,Aslan B,Gürer YK

doi

10.1177/0883073807300299

subject

Has Abstract

pub_date

2007-02-01 00:00:00

pages

228-31

issue

2

eissn

0883-0738

issn

1708-8283

pii

22/2/228

journal_volume

22

pub_type

杂志文章
  • Intracranial cavernomatous hemangiomas as a cause of childhood temporal lobe epilepsy.

    abstract::A 12-year-old boy presented with complaints of seizures since the age of 7 years. Seizure semiology was consistent with origin from the right temporal lobe. Magnetic resonance imaging of the brain revealed a large right temporal and multiple small intracranial cavernomatous hemangiomas. The imaging findings and clinic...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073810371226

    authors: Sharma S,Sankhyan N,Gulati S,Kumar A

    更新日期:2010-11-01 00:00:00

  • Pediatric to Adult Transitions of Ketogenic Dietary Therapy for Epilepsy.

    abstract::Ketogenic therapy is now an accepted treatment for pediatric and adult patients with medically refractory epilepsy.1-3 However, young adults treated with a ketogenic diet face unique challenges when transitioning to adult neurology providers.4 The variable acceptance of dietary therapy, paucity of nutritionists and ad...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073820938587

    authors: Seaborg K,Wang X,Olson C,Felton EA

    更新日期:2020-11-01 00:00:00

  • Respiratory syncytial virus infection and neurologic abnormalities: retrospective cohort study.

    abstract::Respiratory syncytial virus is a common cause of acute respiratory infection in children. Previous reports have associated respiratory syncytial virus infection and acute neurologic symptoms, including apnea and seizures. This study examined the prevalence of acute neurologic symptoms associated with respiratory syncy...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738040190110301

    authors: Kho N,Kerrigan JF,Tong T,Browne R,Knilans J

    更新日期:2004-11-01 00:00:00

  • Pelizaeus-Merzbacher disease and spastic paraplegia type 2: two faces of myelin loss from mutations in the same gene.

    abstract::Pelizaeus-Merzbacher disease and X-linked spastic paraplegia type 2 are two sides of the same coin. Both arise from mutations in the gene encoding myelin proteolipid protein. The disease spectrum for Pelizaeus-Merzbacher disease and spastic paraplegia type 2 is extraordinarily broad, ranging from a spastic gait in the...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/08830738030180090801

    authors: Hudson LD

    更新日期:2003-09-01 00:00:00

  • Mitochondrial DNA deletion in a child with megaloblastic anemia and recurrent encephalopathy.

    abstract::A 3 1/2-year-old boy presented with megaloblastic anemia and recurrent episodes of severe lactic acidosis and coma. At age 4 years, he developed sepsis and died; postmortem examination failed to show any gross abnormality in any tissue. Biochemical analysis of muscle showed decreased activities for all respiratory cha...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380401900403

    authors: Akman CI,Sue CM,Shanske S,Tanji K,Bonilla E,Ojaimi J,Krishna S,Schubert R,DiMauro S

    更新日期:2004-04-01 00:00:00

  • Neurometabolic disorder with microcephaly, dystonia, and central cyanosis masquerading as cerebral palsy.

    abstract::Many neurodegenerative diseases can be misdiagnosed as cerebral palsy. The correct diagnosis is reached when the condition recurs in families or when there are specific clinical signs. The clinical and imaging features of 3 children, from 2 unrelated families, presenting with global developmental delay and dystonia ar...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813512026

    authors: Devadathan K,Sreedharan M,Sarasam S,Colah RB,Kunju PA

    更新日期:2014-11-01 00:00:00

  • Acute pseudobulbar palsy due to bilateral focal cortical damage: the opercular syndrome of Foix-Chavany-Marie.

    abstract::Two children are described who suddenly developed an encephalitic illness with intractable bilateral facial seizures. The seizures subsided over several days, but the children were left with the signs of pseudobulbar palsy and are unable to speak or swallow effectively. Bilateral destructive lesions in the opercular r...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388900400213

    authors: Grattan-Smith PJ,Hopkins IJ,Shield LK,Boldt DW

    更新日期:1989-04-01 00:00:00

  • A Prospective, Crossover Survey Study of Child- and Proxy-Reported Quality of Life According to Spinal Muscular Atrophy Type and Medical Interventions.

    abstract:BACKGROUND:Spinal muscular atrophy is an autosomal-recessive, progressive neuromuscular disease associated with extensive morbidity. Children with spinal muscular atrophy have potentially increased life spans due to improved nutrition, respiratory support, and novel pharmaceuticals. OBJECTIVES:To report on the quality...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073819900463

    authors: Weaver MS,Hanna R,Hetzel S,Patterson K,Yuroff A,Sund S,Schultz M,Schroth M,Halanski MA

    更新日期:2020-04-01 00:00:00

  • Computerized real-time neuromuscular sonography: a new application, techniques and methods.

    abstract::Diagnostic ultrasound has been extensively used for neurologic evaluation of cranial, vascular and spinal diseases. This study presents the techniques, methodology, and procedures for a new diagnostic application of ultrasound for evaluation of the neuromuscular system. In order to determine the optimum sonographic ch...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307388800300115

    authors: Fischer AQ,Stephens S

    更新日期:1988-01-01 00:00:00

  • Congenital Zika Syndrome and Infantile Spasms: Case Series Study.

    abstract::Recently described, the congenital Zika syndrome caused by the Zika virus has many features of other congenital infections. This case series study reports 22 infants with congenital Zika syndrome in Brazil who developed infantile spasms during their first year of life. The median age of infantile spasms onset was 4.3 ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073818780105

    authors: Alves LV,Mello MJG,Bezerra PG,Alves JGB

    更新日期:2018-09-01 00:00:00

  • Scaled Vibratory Feedback Can Bias Muscle Use in Children With Dystonia During a Redundant, 1-Dimensional Myocontrol Task.

    abstract::Vibratory feedback can be a useful tool for rehabilitation. We examined its use in children with dystonia to understand how it affects muscle activity in a population that does not respond well to standard rehabilitation. We predicted scaled vibration (ie, vibration that was directly or inversely proportional to muscl...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073816671830

    authors: Liyanagamage SA,Bertucco M,Bhanpuri NH,Sanger TD

    更新日期:2017-02-01 00:00:00

  • Pathologic basis of the symptomatic epilepsies in childhood.

    abstract::The epilepsies in childhood are classified as primary (or idiopathic) and secondary (or symptomatic). The primary epilepsies account for two thirds of all childhood epilepsies and are presumed to be genetically determined. In the remaining one third of cases, a neuropathologic lesion can be identified. This paper summ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307389801300801

    authors: Armstrong DD,Mizrahi EM

    更新日期:1998-08-01 00:00:00

  • Pyridoxine-dependent seizures associated with hypophosphatasia in a newborn.

    abstract::Pyridoxine dependency and congenital hypophosphatasia are unusual metabolic disorders. We report a female infant born from healthy consanguineous parents with shortening of limbs, detected during pregnancy by ultrasonography. Immediately after delivery, the baby was admitted to the neonatal intensive care unit because...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307380201700314

    authors: Nunes ML,Mugnol F,Bica I,Fiori RM

    更新日期:2002-03-01 00:00:00

  • Schilder's disease: case study with serial neuroimaging.

    abstract::Schilder's myelinoclastic diffuse sclerosis is a rare sporadic demyelinating disease that usually affects children between 5 and 14 years old. The disease often mimics intracranial neoplasm or abscess. We report a 9-year-old girl with Schilder's disease who presented with left hemiparesis. Cranial computed tomography ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738030180011301

    authors: Kurul S,Cakmakçi H,Dirik E,Kovanlikaya A

    更新日期:2003-01-01 00:00:00

  • Epidemiology of Pediatric-Onset Multiple Sclerosis: A Systematic Review of the Literature.

    abstract::Multiple sclerosis onset in youth is increasingly recognized. A systematic review was conducted to assess incidence and prevalence of pediatric-onset multiple sclerosis, focusing on occurrence by age subgroups and disease course. A literature search for the period 1965-2018 was carried out, selecting population-based ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073819845827

    authors: Jeong A,Oleske DM,Holman J

    更新日期:2019-10-01 00:00:00

  • Magnetic resonance imaging (MRI) as a translational tool for the study of neonatal stroke.

    abstract::More than half of neonatal stroke survivors have long-term sequelae, including seizures and neurological deficits. Although the immature brain has tremendous potential for recovery, mechanisms governing repair are essentially unexplored. We investigated whether magnetic resonance imaging (MRI) early or late after tran...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073811408308

    authors: Dzietko M,Wendland M,Derugin N,Ferriero DM,Vexler ZS

    更新日期:2011-09-01 00:00:00

  • Right hemisphere dysfunction in subjects with attention-deficit disorder with and without hyperactivity.

    abstract::The attention-deficit disorder, with and without hyperactivity, is associated with defective attention, response inhibition and, in attention-deficit disorder with hyperactivity, with motor restlessness. In adults, inattention, defective response inhibition, and impersistence are more commonly seen in right hemisphere...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/088307389701200207

    authors: García-Sánchez C,Estévez-González A,Suárez-Romero E,Junqué C

    更新日期:1997-02-01 00:00:00

  • Spasticity in cerebral palsy and the selective posterior rhizotomy procedure.

    abstract::A review of the selective posterior rhizotomy procedure for reduction of spasticity in cerebral palsy is presented. The history of the procedure, selection of patients, operative technique, and results are described. The neurophysiologic basis for spasticity is considered, as well as the role of spasticity in the comp...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/088307389000500303

    authors: Peacock WJ,Staudt LA

    更新日期:1990-07-01 00:00:00

  • Safety and Tolerability of Adjunctive Eslicarbazepine Acetate in Pediatric Patients (Aged 4-17 Years) With Focal Seizures.

    abstract:OBJECTIVE:To evaluate the safety and tolerability of adjunctive eslicarbazepine acetate (ESL) in pediatric patients (aged 4-17 years) with refractory focal seizures. METHODS:Pooled safety data from patients aged 4-17 years in Study 208 (NCT01527513) and Study 305 (NCT00988156) were analyzed. Both were randomized, doub...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073819890997

    authors: Mintz M,Pina-Garza JE,Wolf SM,McGoldrick PE,Józwiak S,Grinnell T,Cantu D,Costa R,Moreira J,Li Y,Blum D

    更新日期:2020-03-01 00:00:00

  • Pilot Testing Behavior Therapy for Chronic Tic Disorders in Neurology and Developmental Pediatrics Clinics.

    abstract::Comprehensive Behavioral Intervention for Tics (CBIT) is an efficacious treatment with limited regional availability. As neurology and pediatric clinics are often the first point of therapeutic contact for individuals with tics, the present study assessed preliminary treatment response, acceptability, and feasibility ...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0883073815599257

    authors: Ricketts EJ,Gilbert DL,Zinner SH,Mink JW,Lipps TD,Wiegand GA,Vierhile AE,Ely LJ,Piacentini J,Walkup JT,Woods DW

    更新日期:2016-03-01 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

  • A child with Diamond-Blackfan anemia, methylenetetrahydrofolate reductase mutation, and perinatal stroke.

    abstract::Diamond-Blackfan anemia is a congenital hypoproliferative anemia known to be associated with diverse physical anomalies affecting the thumb, craniofacial bones, urogenital system, and heart; prematurity; and fetal demise. We report the case of a 16-month-old boy with Diamond-Blackfan anemia noted to have decreased use...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738030180111301

    authors: Butrum MW,Williams LS,Golomb MR

    更新日期:2003-11-01 00:00:00

  • Comorbid Medical Conditions in Friedreich Ataxia: Association With Inflammatory Bowel Disease and Growth Hormone Deficiency.

    abstract::Friedreich ataxia is a progressive degenerative disease with neurologic and cardiac involvement. This study characterizes comorbid medical conditions in a large cohort of patients with Friedreich ataxia. Patient diagnoses were collected in a large natural history study of 641 subjects. Prevalence of diagnoses in the c...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1177/0883073816643408

    authors: Shinnick JE,Schadt K,Strawser C,Wilcox N,Perlman SL,Wilmot GR,Gomez CM,Mathews KD,Yoon G,Zesiewicz T,Hoyle C,Subramony SH,Yiu EM,Delatycki MB,Brocht AF,Farmer JM,Lynch DR

    更新日期:2016-08-01 00:00:00

  • The Yield of Neuroimaging in Children Presenting to the Emergency Department With Acute Ataxia in the Post-Varicella Vaccine Era.

    abstract::To determine the yield of neuroimaging in children presenting to the emergency department with acute ataxia in the post-varicella vaccine era, we conducted a cross-sectional study between 1995 and 2013 at a single pediatric tertiary care center. We included children aged 1-18 years evaluated for acute ataxia of <7 day...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073814561300

    authors: Rudloe T,Prabhu SP,Gorman MP,Nigrovic LE,Harper MB,Landschaft A,Kimia AA

    更新日期:2015-09-01 00:00:00

  • Genetic or Other Causation Should Not Change the Clinical Diagnosis of Cerebral Palsy.

    abstract::High throughput sequencing is discovering many likely causative genetic variants in individuals with cerebral palsy. Some investigators have suggested that this changes the clinical diagnosis of cerebral palsy and that these individuals should be removed from this diagnostic category. Cerebral palsy is a neurodevelopm...

    journal_title:Journal of child neurology

    pub_type: 杂志文章,评审

    doi:10.1177/0883073819840449

    authors: MacLennan AH,Lewis S,Moreno-De-Luca A,Fahey M,Leventer RJ,McIntyre S,Ben-Pazi H,Corbett M,Wang X,Baynam G,Fehlings D,Kurian MA,Zhu C,Himmelmann K,Smithers-Sheedy H,Wilson Y,Ocaña CS,van Eyk C,Badawi N,Wintle RF,Ja

    更新日期:2019-07-01 00:00:00

  • Growth patterns in children with intrauterine growth retardation and their correlation to neurocognitive development.

    abstract::The relationship between somatic growth and neurocognitive outcome was studied in a cohort of 136 children with intrauterine growth retardation. The children were followed up from birth to 9 to 10 years of age by annual measurements of growth parameters, neurodevelopmental evaluations, and IQ. The rate of catch-up for...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808331082

    authors: Fattal-Valevski A,Toledano-Alhadef H,Leitner Y,Geva R,Eshel R,Harel S

    更新日期:2009-07-01 00:00:00

  • Correlation of brain ultrasonography scans to the neuromotor outcome of very-low-birth-weight infants during the first year of life.

    abstract::To evaluate the consistency of the Hammersmith Infant Neurological Examination scores of very-low-birth-weight infants at 6 and 12 months of age and its correlation to cranial ultrasonography findings, we designed a prospective study between January 2005 and January 2008, in the tertiary Neonatal Unit of Aristotle Uni...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073813479171

    authors: Karagianni P,Rallis D,Kyriakidou M,Tsakalidis C,Pratsiou P,Nikolaidis N

    更新日期:2014-11-01 00:00:00

  • Practical aspects of conducting large-scale functional magnetic resonance imaging studies in children.

    abstract::The potential benefits of functional magnetic resonance imaging (MRI) for the investigation of normal development have been limited by difficulties in its use with children. We describe the practical aspects, including failure rates, involved in conducting large-scale functional MRI studies with normal children. Two h...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/08830738020170122201

    authors: Byars AW,Holland SK,Strawsburg RH,Bommer W,Dunn RS,Schmithorst VJ,Plante E

    更新日期:2002-12-01 00:00:00

  • Unusual manifestations of pediatric neuromyelitis optica.

    abstract::Neuromyelitis optica is a rare, severe idiopathic disease that predominantly involves optic nerves and spinal cord. Main clinical features of neuromyelitis optica are visual loss, paraparesis or tetraparesis, sensory loss, and sphincter dysfunction. A 13-year-old girl with vision loss and behavioral change was admitte...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073812448837

    authors: Yavuz H,Kiresi D

    更新日期:2013-05-01 00:00:00

  • Successful treatment of cytomegalovirus polyradiculopathy in a 9-year-old child with congenital human immunodeficiency virus infection.

    abstract::Cytomegalovirus lumbosacral polyradiculopathy is a well-documented complication of human immunodeficiency virus in adults who have a CD4 count of less than 40/microL. Patients present with an acute ascending flaccid paralysis of the lower limbs with areflexia, paresthesia, and urinary and bowel symptoms. However, it a...

    journal_title:Journal of child neurology

    pub_type: 杂志文章

    doi:10.1177/0883073808322671

    authors: Sohal A,Riordan A,Mallewa M,Solomon T,Kneen R

    更新日期:2009-02-01 00:00:00