keyword
https://read.qxmd.com/read/38621190/very-long-term-functional-outcomes-and-dependency-in-children-with-anti-nmda-receptor-encephalitis
#21
JOURNAL ARTICLE
Li-Wen Chen, Gemma Olivé-Cirera, Elianet G Fonseca, Mateus Mistieri Simabukuro, Takahiro Iizuka, Thais Armangue, Josep Dalmau
OBJECTIVES: To assess the daily function of children with anti-N-methyl-d-aspartate receptor encephalitis (NMDARe) after a minimal follow-up of 5 years. METHODS: Patients 18 years and younger by the time of disease onset, whose serum and CSF were studied in our center between 2013 and 2017, were included in the study. Patients' daily life function was assessed by their physicians using a 15-domain question format (Liverpool Outcome Score). RESULTS: Of 76 patients, 8 (11%) died and 68 were followed for a mean of 7...
May 2024: Neurology® Neuroimmunology & Neuroinflammation
https://read.qxmd.com/read/38618871/sources-of-pharmacokinetic-and-pharmacodynamic-variability-and-clinical-pharmacology-studies-of-antiseizure-medications-in-the-pediatric-population
#22
REVIEW
Patricia D Maglalang, Jiali Wen, Christoph P Hornik, Daniel Gonzalez
Multiple treatment options exist for children with epilepsy, including surgery, dietary therapies, neurostimulation, and antiseizure medications (ASMs). ASMs are the first line of therapy, and more than 30 ASMs have U.S. Food and Drug Administration (FDA) approval for the treatment of various epilepsy and seizure types in children. Given the extensive FDA approval of ASMs in children, it is crucial to consider how the physiological and developmental changes throughout childhood may impact drug disposition. Various sources of pharmacokinetic (PK) variability from different extrinsic and intrinsic factors such as patients' size, age, drug-drug interactions, and drug formulation could result in suboptimal dosing of ASMs...
April 2024: Clinical and Translational Science
https://read.qxmd.com/read/38618670/-guide-for-the-treatment-of-acute-altered-mental-status-iberoamerican-academy-of-pediatric-neurology
#23
D López, F Espinel, E Andrade, A S Aguirre
In pediatric patients, an acute altered mental status refers to a sudden and significant change in a child's brain function and level of consciousness. It may manifest as confusion, disorientation, agitation, lethargy or even a loss of consciousness. This condition is a medical emergency, and requires immediate evaluation and attention. There are several causes of acute altered mental status in children, including infections of the central nervous system such as meningitis or encephalitis, traumatic brain injury, metabolic disorders, seizures and poisoning, among others...
April 16, 2024: Revista de Neurologia
https://read.qxmd.com/read/38618391/effects-of-pediatric-rehabilitation-on-children-with-spastic-quadriplegia-primary-to-seizure-disorder-and-global-developmental-delay-a-case-report
#24
Neha M Chitlange, H V Sharath, Akshaya Saklecha, Sakshi Desai
The most severe form of spastic cerebral palsy (CP), which affects the arms and legs and often the face, is known as spastic quadriplegia. In addition to other developmental disabilities such as intellectual disability and seizures, it can cause difficulty in walking. Children with CP often have seizures as a result of brain injury, and spastic quadriplegic CP is typically associated with global developmental delay. For the purpose of addressing the unique motor and functional challenges associated with spastic quadriplegia, neurophysiotherapy is essential...
March 2024: Curēus
https://read.qxmd.com/read/38617397/risk-factors-of-seizure-in-childhood-shigellosis
#25
JOURNAL ARTICLE
Abolfazl Mahyar, Shifteh Mahyar, Sonia Oveisi, Bahman Khajeh, Khatereh Khamenehpour, Victoria Chegini, Reza Dalirani, Mojgan Enadi, Shiva Esmaeili
OBJECTIVES: Shigellosis is one of the common causes of bacterial diarrhea in children. Seizures are common in shigellosis. It is essential to identify the risk factors of seizure in this disease. MATERIALS & METHODS: This study was conducted on 224 children with shigellosis. The patients were divided into: With (case groups = 63 cases) and without seizures (control group = 161 cases). Groups were compared regarding different variables such as age, gender, clinical symptoms, and laboratory findings...
2024: Iranian Journal of Child Neurology
https://read.qxmd.com/read/38617391/gm1-and-gm2-gangliosidosis-clinical-features-neuroimaging-findings-and-electroencephalography
#26
JOURNAL ARTICLE
Parvaneh Karimzadeh, Masomeh Ebrahimi, Korosh Etemad, Farzad Ahmad Abadi, Zahra Hosseini Nezhad
ABSTRACT: Gangliosidosis is one of the hereditary metabolic diseases caused by the accumulation of Gangliosid in the central nervous system, leading to severe and progressive neurological deficits. Regarding phenotype, GM1 and GM2-Gangliosidosis are divided into Infantile, Juvenile, and Adult. MATERIALS & METHODS: In this study, thirty-seven patients with GM1 and GM2-Gangliosidosis were referred to the neurology department of Mofid Children's Hospital in Tehran, Iran, whose disease was confirmed from September 2019 to December 2021...
2024: Iranian Journal of Child Neurology
https://read.qxmd.com/read/38613879/using-scalp-eeg-to-predict-seizure-recurrence-and-electrical-status-epilepticus-in-children-with-idiopathic-focal-epilepsy
#27
JOURNAL ARTICLE
Xiaofei Ye, Panpan Hu, Bin Yang, Yang Yang, Ding Gao, Ginger Qinghong Zeng, Kai Wang
PURPOSE: Some individuals with idiopathic focal epilepsy (IFE) experience recurring seizures accompanied by the evolution of electrical status epilepticus during sleep (ESES). Here, we aimed to develop a predictor for the early detection of seizure recurrence with ESES in children with IFE using resting state electroencephalogram (EEG) data. METHODS: The study group included 15 IFE patients who developed seizure recurrence with ESES. There were 17 children in the control group who did not experience seizure recurrence with ESES during at least 2-year follow-up...
March 27, 2024: Seizure: the Journal of the British Epilepsy Association
https://read.qxmd.com/read/38613877/association-of-minor-electrocardiographic-ecg-abnormalities-with-epilepsy-duration-in-children-a-manifestation-of-the-epileptic-heart
#28
JOURNAL ARTICLE
Brittnie Bartlett-Lee, Leslie Dervan, Christina Miyake, R Scott Watson, See Wai Chan, Anne E Anderson, Yi-Chen Lai
PURPOSE: Cardiac abnormalities resulting from chronic epilepsy ("the epileptic heart") constitute a well-recognized comorbidity. However, the association of cardiac alterations with epilepsy duration remains understudied. We sought to evaluate this association using electrocardiogram (ECG). METHODS: We prospectively enrolled children between 1 months and 18 years of age without known cardiac conditions or ion channelopathies during routine clinic visits. ECGs were categorized as abnormal if there were alterations in rhythm; PR, QRS, or corrected QT interval; QRS axis or morphology; ST segment or T wave...
April 10, 2024: Seizure: the Journal of the British Epilepsy Association
https://read.qxmd.com/read/38613366/original-research-clinical-significance-of-a-unique-pediatric-eeg-configuration-bi-frontal-spikes-with-simultaneous-bi-occipital-positivity
#29
JOURNAL ARTICLE
Jacqueline Crawford, Cassie McFarlane, Anita N Datta
Introduction: Frontal-predominant epileptiform discharges (EDs) include generalized spike-wave (GSW) and frontal spikes (FS). However, negative bi-frontal ED with simultaneous occipital positivity (BFOD) are rare, leading to questions regarding physiological generators. Methods: To determine the clinical significance of BFOD, electroclinical features of children with BFOD (n = 40) were compared to control patients with GSW (n = 102) and FS (n = 100). Results: Results are presented in the following order: BFOD, GSW, and FS...
April 13, 2024: Clinical EEG and Neuroscience: Official Journal of the EEG and Clinical Neuroscience Society (ENCS)
https://read.qxmd.com/read/38608552/a-comprehensive-examination-of-clinical-characteristics-and-determinants-of-long-term-outcomes-in-pediatric-cerebral-sinus-venous-thrombosis
#30
JOURNAL ARTICLE
Cemal Karakas, Isabella Herman, Stephen F Kralik, Troy A Webber, Danielle S Takacs, Saleh Bhar, Davut Pehlivan
BACKGROUND: To analyze the clinical and neuroimaging features, risk factors, treatment choices, and long-term clinical outcomes in children with cerebral sinus venous thrombosis (CSVT). METHODS: This is a retrospective cohort study of children diagnosed with CSVT between 2002 and 2018 at Texas Children's Hospital. RESULTS: A total of 183 children (male: 62.3%) with CSVT were included. The average presenting age was 7.7 years (S.D.: 5...
March 26, 2024: Pediatric Neurology
https://read.qxmd.com/read/38608307/responsive-neurostimulation-of-thalamic-nuclei-for-regional-and-multifocal-drug-resistant-epilepsy-in-children-and-young-adults
#31
JOURNAL ARTICLE
Deepankar Mohanty, Kimberly M Houck, Cristina Trandafir, Zulfi Haneef, Cemal Karakas, Steven Lee, Daniel J Curry, James J Riviello, Irfan Ali
OBJECTIVE: Responsive neurostimulation (RNS) is a US FDA-approved form of neuromodulation to treat patients with focal-onset drug-resistant epilepsy (DRE) who are ineligible for or whose condition is refractory to resection. However, the FDA approval only extends to use in patients with one or two epileptogenic foci. Recent literature has shown possible efficacy of thalamic RNS in patients with Lennox-Gastaut syndrome and multifocal epilepsy. The authors hypothesized that RNS of thalamic nuclei may be effective in seizure reduction for patients with multifocal or regionalized-onset DRE...
April 12, 2024: Journal of Neurosurgery. Pediatrics
https://read.qxmd.com/read/38608010/clozapine-treatment-for-aggressive-behaviors-in-youths-with-neurodevelopmental-disorders
#32
JOURNAL ARTICLE
Stefano Berloffa, Gabriele Masi, Francesca Falcone, Valerio Simonelli, Antonio Narzisi, Elena Valente, Valentina Viglione, Annarita Milone, Gianluca Sesso
Objectives: The aim of this study was to assess effectiveness and tolerability of Clozapine in the treatment of aggression in youth with Neurodevelopmental Disorders. Methods: Patients were consecutively admitted at our third-level university hospital with nationwide catchment from June 2018 to October 2022, and followed up to July 2023. Eligibility criteria were as follows: (1) Autism Spectrum Disorder (ASD) and/or Intellectual Disability/Borderline Cognitive Functioning, (2) behavioral dyscontrol with physical aggression; (3) age range between 8 and 18 years; (4) clinical indication for Clozapine treatment after at least two failed trials with other Second-Generation Antipsychotics (SGAs); (5) availability of an at least 6-month-long follow-up...
April 2024: Journal of Child and Adolescent Psychopharmacology
https://read.qxmd.com/read/38607549/giant-cerebral-cavernous-malformation-in-a-newborn-a-rare-case-report-and-review-of-literature
#33
JOURNAL ARTICLE
Ismael Moreno, Gianluca Scalia, Giuseppe Emmanuele Umana, Ciro Soriano, Isis Alcivar, Bipin Chaurasia
BACKGROUND: Cavernous malformations (CMs), also known as cavernomas or cavernous angiomas, are vascular malformations characterized by sinusoidal spaces lined by endothelial cells. Giant CMs (GCMs) are extremely rare, with limited understanding of their presentation and management. We present a case of symptomatic GCM in a newborn and review the literature on this rare entity. CASE DESCRIPTION: A 1-month-old newborn presented with focal seizures and signs of increased intracranial pressure...
April 12, 2024: Child's Nervous System: ChNS: Official Journal of the International Society for Pediatric Neurosurgery
https://read.qxmd.com/read/38606683/ethosuximide-lowers-lamotrigine-serum-concentrations-evidence-for-a-clinically-relevant-interaction
#34
JOURNAL ARTICLE
Anne Hagemann, Arne Herting, Dennis Klimpel, Christian G Bien, Tilman Polster
We investigated the effect of comedication with ethosuximide (ESM) on lamotrigine (LTG) blood levels. Based on observations from clinical practice, we hypothesized that ESM reduces the LTG serum concentration. We additionally evaluated this effect in the presence of concomitant valproic acid (VPA). We retrospectively analyzed samples of inpatients from our department who had been treated with a combination of ESM and LTG between 2017 and 2021. We additionally used data on LTG serum concentrations from a previously published cohort from our center...
April 12, 2024: Epilepsia
https://read.qxmd.com/read/38603939/applicability-of-the-international-league-against-epilepsy-ilae-2022-diagnostic-criteria-for-epilepsy-syndromes-in-children-a-retrospective-review-of-1550-children-with-epilepsy
#35
JOURNAL ARTICLE
Bhavya Kansal, Aakanksha Anand, Divyani Garg, Anshika Gupta, Ashna Kumar, Suvasini Sharma
OBJECTIVE: Recently, the ILAE Nosology and Definitions Task Force defined diagnostic criteria for epilepsy syndromes. There is paucity of data on the use of these new diagnostic criteria in children with epilepsy, and how these criteria may lead to changes from previous practice. METHODS: This was a retrospective chart review of data of children attending the epilepsy clinic in a tertiary care children's hospital from January 2011 to January 2023. The clinical details such as age at onset, types of seizures, co-morbidities, and results of EEG, MRI and genetic testing were reviewed...
March 27, 2024: Seizure: the Journal of the British Epilepsy Association
https://read.qxmd.com/read/38600595/additive-interaction-between-birth-asphyxia-and-febrile-seizures-on-autism-spectrum-disorder-a-population-based-study
#36
JOURNAL ARTICLE
Yi Mao, Xindi Lin, Yuhan Wu, Jiayi Lu, Jiayao Shen, Shaogen Zhong, Xingming Jin, Jun Ma
BACKGROUND: Autism Spectrum Disorder (ASD) is a pervasive neurodevelopmental disorder that can significantly impact an individual's ability to socially integrate and adapt. It's crucial to identify key factors associated with ASD. Recent studies link both birth asphyxia (BA) and febrile seizures (FS) separately to higher ASD prevalence. However, investigations into the interplay of BA and FS and its relationship with ASD are yet to be conducted. The present study mainly focuses on exploring the interactive effect between BA and FS in the context of ASD...
April 10, 2024: Molecular Autism
https://read.qxmd.com/read/38595362/contemporary-insights-into-intractable-epilepsy-in-children
#37
JOURNAL ARTICLE
Khaled Saad, Emad H Eldaly, Hazem M Abdelall, Nahed M Abdelgabaar, David M Zaki, Hamad G Dailah, Ahmed Shams-Eldeen, Khalid H Mahmoud
While most children with epilepsy find their seizures manageable through medication, some continue to experience seizures despite trying multiple drugs. Failure of medical treatment often becomes apparent early on, and for these cases, it is advisable to seek further treatment options at a specialized epilepsy center. Such centers offer additional treatments like epilepsy surgery, vagus nerve stimulation, and ketogenic diets. There is no universal definition for what constitutes "medically intractable" epilepsy...
February 2024: Journal of Pharmacy & Bioallied Sciences
https://read.qxmd.com/read/38594715/clinical-functional-correlation-with-brain-volumetry-in-severe-perinatal-asphyxia-a-case-report
#38
JOURNAL ARTICLE
Juan Pablo Velasquez-Minoli, Natalia Cardona-Ramirez, Hernan Felipe Garcia-Arias, Feliza Restrepo-Restrepo, Gloria Liliana Porras-Hurtado
BACKGROUND: Hypoxic-ischemic encephalopathy (HIE) appears in neurological conditions where some brain areas are likely to be injured, such as deep grey matter, basal ganglia area, and white matter subcortical periventricular áreas. Moreover, modeling these brain areas in a newborn is challenging due to significant variability in the intensities associated with HIE conditions. This paper aims to evaluate functional measurements and 3D machine learning models of a given HIE case by correlating the affected brain areas with the pathophysiology and clinical neurodevelopmental...
April 9, 2024: Italian Journal of Pediatrics
https://read.qxmd.com/read/38592426/hearing-loss-in-baraitser-winter-syndrome-case-reports-and-review-of-the-literature
#39
REVIEW
Sara Ghiselli, Giulia Parmeggiani, Giulia Zambonini, Domenico Cuda
Background : Baraitser-Winter Syndrome (BRWS) is a rare autosomal dominant condition associated with hearing loss (HL). In the literature, two types of this condition are reported, Baraitser-Winter type 1 (BRWS1) and type 2 (BRWS2) produced by specific pathogenetic variants of two different genes, ACTB for BRWS1 and ACTG1 for BRWS2. In addition to syndromic BRWS2, some pathogenic variants in ACTG1 are associated also to another pathologic entity, the "Autosomal dominant non-syndromic hearing loss 20/26". In these syndromes, typical craniofacial features, sensory impairment (vision and hearing) and intellectual disabilities are frequently present...
March 5, 2024: Journal of Clinical Medicine
https://read.qxmd.com/read/38591353/recent-advances-in-understanding-the-neurobiology-of-pediatric-functional-neurological-disorder
#40
REVIEW
Kasia Kozlowska, Stephen Scher
INTRODUCTION: Functional neurological disorder (FND) is a neuropsychiatric disorder that manifests in a broad array of functional motor, sensory, or cognitive symptoms, which arise from complex interactions between brain, mind, body, and context. Children with FND make up 10%-20% of presentations to neurology services in children's hospitals and up to 20% of adolescents admitted to hospital for the management of intractable seizures. AREAS COVERED: The current review focuses on the neurobiology of pediatric FND...
April 9, 2024: Expert Review of Neurotherapeutics
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