Search results for "Epilepsy"

showing 10 items of 420 documents

Lateralized periodic discharges in insular status epilepticus: A case report of a periodic EEG pattern associated with ictal manifestation

2019

Highlights • Focal status epilepticus has to be considered in the differential diagnosis of patients presenting with aphasia, even in the absence of previous history of epilepsy. • Aphasia can be a rare presenting sign of insular lobe epilepsy. • Lateralized periodic discharges could represent an EEG ictal pattern.

Hypersalivationmedicine.medical_specialtyInsular epilepsyLPDs + FStatus epilepticusAudiologybehavioral disciplines and activitieslcsh:RC321-57103 medical and health sciencesEpilepsy0302 clinical medicinePhysiology (medical)AphasiaMedicineIctalPathologicallcsh:Neurosciences. Biological psychiatry. Neuropsychiatrybusiness.industryBrain tumuor030208 emergency & critical care medicinemedicine.diseaseLobenervous system diseasesFocal status epilepticusmedicine.anatomical_structurenervous systemNeurologyClinical and Research ArticleSettore MED/26 - NeurologiaNeurology (clinical)medicine.symptomDifferential diagnosisbusiness030217 neurology & neurosurgery
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Congenital generalized hypertrichosis: the skin as a clue to complex malformation Syndromes.

2015

Hypertrichosis is defined as an excessive growth in body hair beyond the normal variation compared with individuals of the same age, race and sex and affecting areas not predominantly androgen-dependent. The term hirsutism is usually referred to patients, mainly women, who show excessive hair growth with male pattern distribution. Hypertrichosis is classified according to age of onset (congenital or acquired), extent of distribution (generalized or circumscribed), site involved, and to whether the disorder is isolated or associated with other anomalies. Congenital hypertrichosis is rare and may be an isolated condition of the skin or a component feature of other disorders. Acquired hypertri…

HypertrichosisPediatricsmedicine.medical_specialtybusiness.industryHypertrichosisGenetic Diseases X-LinkedAdrenal neoplasmSyndromeReviewmedicine.diseaseSettore MED/03 - GENETICA MEDICABody hairEpilepsyCongenital generalized hypertrichosisAnorexia nervosa (differential diagnoses)Pediatrics Perinatology and Child HealthmedicineHumansEndocrine systemAge of onsetbusinesshirsutismSkin
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Kohlschütter-Tönz Syndrome: report of an additional case

2013

Kohlschütter-Tönz Syndrome is a rare disorder clinically characterized by amelogenesis imperfecta, epilepsy and progressive mental deterioration. We present an additional case of this syndrome of a nine year-old boy who was referred by pigmented teeth. The mental deterioration was associated with speech delay, impulsive behavior, attention-deficit/hyperactivity disorder, and learning problems. The physical examination revealed a reduction of lower third, slightly palpebral fissures, low ear and hair implantation, coarse hair and hypertrichosis. The intraoral examination showed alteration in teeth pigmentation diagnosed as amelogenesis imperfecta. Although rare, the present case report illus…

Hypertrichosismedicine.medical_specialtyDentistryCase ReportPhysical examinationOdontologíaKohlschütter-Tönz syndromeEpilepsymedicineAmelogenesis imperfectaGeneral DentistryOral Medicine and Pathologymedicine.diagnostic_testMental deteriorationbusiness.industry:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseDermatologyCiencias de la saludstomatognathic diseasesPalpebral fissureSpeech delayUNESCO::CIENCIAS MÉDICASmedicine.symptombusiness
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A Framework to Assess the Information Dynamics of Source EEG Activity and Its Application to Epileptic Brain Networks

2020

This study introduces a framework for the information-theoretic analysis of brain functional connectivity performed at the level of electroencephalogram (EEG) sources. The framework combines the use of common spatial patterns to select the EEG components which maximize the variance between two experimental conditions, simultaneous implementation of vector autoregressive modeling (VAR) with independent component analysis to describe the joint source dynamics and their projection to the scalp, and computation of information dynamics measures (information storage, information transfer, statistically significant network links) from the source VAR parameters. The proposed framework was tested on…

Information transfercommon spatial patternComputer science0206 medical engineeringcommon spatial patterns02 engineering and technologyElectroencephalographyInformation theoryArticlelcsh:RC321-57103 medical and health sciencesEpilepsy0302 clinical medicineinformation storagemedicineinformation transferIctalEEGGeneralized epilepsylcsh:Neurosciences. Biological psychiatry. Neuropsychiatryinformation theorymedicine.diagnostic_testbusiness.industryGeneral NeurosciencePattern recognitionmedicine.disease020601 biomedical engineeringIndependent component analysismedicine.anatomical_structurevector autoregressive modelingindependent component analysisScalpSettore ING-INF/06 - Bioingegneria Elettronica E InformaticaepilepsyArtificial intelligencebusiness030217 neurology & neurosurgeryBrain Sciences
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Les accidents vasculaires cérébraux du nouveau-né et de l’enfant

2009

The clinical presentation, risk factors, causes, vital or functional prognosis, and acute management options for stroke occurring in neonates and children are specific, differing from those observed in young adults. Compared with the adult population, less is known about the epidemiology of stroke in the under-18 population where the disease could become more frequent because of advances in both neonatal resuscitation techniques for cerebral disorders and neuroimaging techniques enabling the diagnosis of small lesions. Clinical features are often delayed, especially in neonates, and unlike epilepsy or dystonia of the affected limb, which are frequent complications, aphasia is rather rare. T…

Intracerebral hemorrhageeducation.field_of_studymedicine.medical_specialtyPediatricsbusiness.industryPopulationDiseasemedicine.diseaseEpilepsyNeurologyEpidemiologyMedicineNeurology (clinical)Risk factorbusinesseducationStrokeNeonatal resuscitationRevue Neurologique
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The Endocannabinoid System as a Therapeutic Target in Epilepsy

2008

Kainic acidbusiness.industryStatus epilepticusmedicine.diseaseGABAergic neuronEndocannabinoid systemEpilepsychemistry.chemical_compoundchemistryFebrile seizureMedicinemedicine.symptombusinessNeuroscience
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De novo GRIN2A variants associated with epilepsy and autism and literature review

2021

N-methyl-D-aspartate receptors (NMDAR) are di- or tri-heterotetrameric ligand-gated ion channels composed of two obligate glycine-binding GluN1 subunits and two glutamate-binding GluN2 or GluN3 subunits, encoded by GRIN1, GRIN2A–D, and GRIN3A–B receptor genes respectively. Each NMDA receptor subtype has different temporal and spatial expression patterns in the brain and varies in the cell types and subcellular localization resulting in different functions. They play a crucial role in mediating the excitatory neurotransmission, but are also involved in neuronal development and synaptic plasticity, essential for learning, memory, and high cognitive functions. Among genes coding NMDAR subunits…

Landau-Kleffner SyndromeEpilepsySettore M-PSI/02 - Psicobiologia E Psicologia FisiologicaIntellectual disabilityGRIN2BGRIN2AReceptors N-Methyl-D-AspartateGene de novo variantsSettore MED/39 - Neuropsichiatria InfantileBehavioral NeuroscienceSettore MED/38 - Pediatria Generale E SpecialisticaNeurologyNeurodevelopmental DisordersSettore M-PSI/08 - Psicologia ClinicaHumansEpilepsies PartialNeurology (clinical)Autism spectrum disorderAutistic DisorderChildEpilepsy & Behavior
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Giant subcutaneous lipomatosis in Myoclonic Epilepsy with Ragged Red Fibers syndrome: The first literature report of “laparoscopic” excision

2020

Background MERRF (Myoclonic Epilepsy with Ragged Red Fibers) is a rare multisystem clinical disorder due to a pathogenic variant of the mitochondrial DNA. Rare symptoms of MERRF include multiple systemic lipomatosis with symmetric uncapsulated lipomas occurs generally on the posterior cervical region and upper back. Methods We report the clinical case of a 46 years-old Caucasian man with MERRF syndrome who presented with MSL on the right cervical region. We decided to perform a mini-invasive approach using laparoscopic instruments. We performed a 10-mm incision about 5 cm under the mass and conducted a blunt dissection of the subcutaneous plane. Then we positioned a 10-mm port and started C…

Laparoscopic surgerymedicine.medical_specialtySubcutaneous lipomatosisbusiness.industryMERRF syndromemedicine.medical_treatmentLipomatosisMini-invasive surgeryMERRF syndromelcsh:Surgerylcsh:RD1-811Laparoscopic excisionLaparoscopic surgerymedicine.diseaseSurgeryMini invasive surgerySettore MED/18 - Chirurgia GeneraleRagged-red fibersSubcutaneous lipomatosismedicineMyoclonic epilepsySurgeryVideoassisted surgerybusiness
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Malformations of Cortical Development and Neocortical Focus

2014

Abstract Developmental neocortical malformations resulting from abnormal neurogenesis, disturbances in programmed cell death, or neuronal migration disorders may cause a long-term hyperexcitability. Early generated Cajal–Retzius and subplate neurons play important roles in transient cortical circuits, and structural/functional disorders in early cortical development may induce persistent network disturbances and epileptic disorders. In particular, depolarizing GABAergic responses are important for the regulation of neurodevelopmental events, like neurogenesis or migration, while pathophysiological alterations in chloride homeostasis may cause epileptic activity. Although modern imaging tech…

LesionElectrophysiologymedicine.anatomical_structureFocus (geometry)Cerebral cortexSubplateNeurogenesismedicineGABAergicEpilepsy surgeryBiologymedicine.symptomNeuroscience
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Subventricular zone neural progenitors protect striatal neurons from glutamatergic excitotoxicity.

2012

The functional significance of adult neural stem and progenitor cells in hippocampal-dependent learning and memory has been well documented. Although adult neural stem and progenitor cells in the subventricular zone are known to migrate to, maintain and reorganize the olfactory bulb, it is less clear whether they are functionally required for other processes. Using a conditional transgenic mouse model, selective ablation of adult neural stem and progenitor cells in the subventricular zone induced a dramatic increase in morbidity and mortality of central nervous system disorders characterized by excitotoxicity-induced cell death accompanied by reactive inflammation, such as 4-aminopyridine-i…

LipopolysaccharidesPolyunsaturated AlkamidesSubventricular zoneGlutamic AcidMice TransgenicArachidonic AcidsBiologyAmidohydrolasesGlutamatergicMiceNeural Stem CellsLateral VentriclesmedicineAnimalsDronabinolProgenitor cell4-Aminopyridineneurogenesis; ischaemia; neural stem cells; excitotoxicity; endocannabinoidsGanciclovirEpilepsyStem CellsNeurogenesisExcitatory Postsynaptic PotentialsNeural stem cellCorpus StriatumNeuroepithelial cellMice Inbred C57BLStrokeneurogenesisDisease Models Animalmedicine.anatomical_structureNeuroprotective AgentsBenzamidesSettore MED/26 - NeurologiaNeurology (clinical)ischaemiaCarbamatesStem cellNeuroscienceexcitotoxicityExcitatory Amino Acid AntagonistsAdult stem cellEndocannabinoidsBrain : a journal of neurology
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