Search results for "Neuropsichiatria infantile"

showing 10 items of 201 documents

Ischemic hypoxic encephalopathy: The role of MRI of neonatal injury and medico-legal implication

2021

Hypoxic ischemic encephalopathy is one of the major causes of neonatal death and neurological disability in the child, and represents the most common birth injury claim. Intrapartum asphyxia often leads to several long-term sequalae, such as cerebral palsy and/or developmental delay, epilepsy. Through the neuroimaging it's possible to identify and define the different lesioned pictures and provide useful elements to establish the moment in which the damage occurred; indeed, timing of injury is a key element in the legal arena. Magnetic resonance imaging (MRI) is emerging as one of the most important tools in identifying the etiologic of neonatal encephalopathy as well as in predicting long-…

Malemedicine.medical_specialtyNeuroimagingHypoxic Ischemic EncephalopathyPathology and Forensic MedicineCerebral palsyMedico-legalEpilepsySettore MED/38 - Pediatria Generale E SpecialisticaNeuroimagingSettore MED/43 - Medicina LegaleMalpractice litigationMalpracticemedicineHumansIschemic Hypoxic encephalopathyIntensive care medicineAsphyxia Neonatorummedicine.diagnostic_testNeonatal encephalopathybusiness.industryInfant NewbornInfantMagnetic resonance imagingForensic Medicinemedicine.diseaseMagnetic Resonance ImagingBirth injurySettore MED/39 - Neuropsichiatria InfantileItalyMRI brainHypoxia-Ischemia BrainCerebral palsyFemalebusinessSettore MED/36 - Diagnostica Per Immagini E RadioterapiaLawHuman
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West syndrome followed by juvenile myoclonic epilepsy: a coincidental occurrence?

2013

Background: West syndrome is an age-dependent epilepsy with onset peak in the first year of life whose aetiology may be symptomatic or cryptogenic. Long-term cognitive and neurological prognosis is usually poor and seizure outcome is also variable. Over the past two decades a few patients with favourable cognitive outcome and with total recovery from seizures were identified among the cryptogenic group suggesting an idiopathic aetiology. Recent research has described two children with idiopathic WS who later developed a childhood absence epilepsy. Case presentation: We reviewed the medical records of patients with West syndrome admitted to the our Child Neuropsychiatry Unit in the last 15 y…

Malemedicine.medical_specialtyPediatricsNeurologyLevetiracetamAdolescentHairy elbows syndromeMyoclonic JerkClinical NeurologyCase ReportEpilepsyChildhood absence epilepsyJuvenile myoclonic epilepsySettore M-PSI/08 - Psicologia ClinicamedicineHumansEpilepsy evolutionPsychiatrySettore M-PSI/02 - Psicobiologia E Psicologia Fisiologicabusiness.industryGenetic predispositionMyoclonic Epilepsy JuvenileBrainInfantWest SyndromeGeneral MedicineWest syndromemedicine.diseaseMagnetic Resonance ImagingPiracetamSettore MED/39 - Neuropsichiatria InfantileWest syndrome Juvenile myoclonic epilepsy Epilepsy evolution Genetic predisposition Hairy elbows syndromeDisease ProgressionMyoclonic epilepsyNeurology (clinical)LevetiracetamJuvenile myoclonic epilepsybusinessSpasms Infantilemedicine.drugBMC neurology
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Reading–writing disorder in children with idiopathic epilepsy

2020

Abstract Several studies have documented learning disabilities (LDs) in subjects with epilepsy, who have been shown to be at greater risk of mild neuropsychological damage, with the consequent risk of academic failure. This retrospective study aimed to investigate the peculiarities of reading and writing disorders in subjects with idiopathic epilepsy. The reading and writing performance of 35 children affected by reading and writing disorders and idiopathic epilepsy (R/WD + E group) has been compared with the performance of 37 children with only reading and writing disorders (R/WD group). A comparison group of 22 typical developing healthy children (TDC group) was also included in the study…

Malemedicine.medical_specialtymedia_common.quotation_subjectWritingeducationShort-term memoryAudiologyNeuropsychological TestsWriting disorderDyslexiaEpilepsy Reading Short-term memory Writing disorder03 medical and health sciencesBehavioral NeuroscienceEpilepsy0302 clinical medicineReading (process)Memory spanmedicineHumansShort-term memory030212 general & internal medicineChildmedia_commonRetrospective StudiesEpilepsyDictationLearning DisabilitiesDyslexiaNeuropsychologymedicine.diseaseSettore MED/39 - Neuropsichiatria InfantileMemory Short-TermNeurologyLearning disabilityFemaleNeurology (clinical)medicine.symptomReading disorderPsychologyReading disorder Writing disorder Epilepsy Short-term memory030217 neurology & neurosurgery
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Evidence for reading improvement following tDCS treatment in children and adolescents with Dyslexia.

2016

Purpose There is evidence that non-invasive brain stimulation transitorily modulates reading by facilitating the neural pathways underactive in individuals with dyslexia. The study aimed at investigating whether multiple sessions of transcranial direct current stimulation (tDCS) would enhance reading abilities of children and adolescents with dyslexia and whether the effect is long-lasting. Methods Eighteen children and adolescents with dyslexia received three 20-minute sessions a week for 6 weeks (18 sessions) of left anodal/right cathodal tDCS set at 1 mA over parieto-temporal regions combined with a cognitive training. The participants were randomly assigned to the active or the sham tre…

Malemedicine.medical_treatmentAudiologyTranscranial Direct Current StimulationFunctional LateralityDevelopmental psychologycognitive trainingDyslexia0302 clinical medicineReading (process)Childmedia_commonneurology (clinical)Cerebral CortexTranscranial direct-current stimulation05 social sciencesCognitive trainingparieto-temporal regionsCognitive behavioral therapyTreatment OutcomeTolerabilityFemaleBrain stimulation cognitive training parieto-temporal regions Adolescent Cerebral Cortex Cognitive Behavioral Therapy Double-Blind Method Dyslexia Functional Laterality Transcranial Direct Current Stimulation Treatment Outcome ReadingPsychologymedicine.medical_specialtyAdolescentmedia_common.quotation_subjectbrain stimulation050105 experimental psychologyNObrain stimulation; cognitive training; parieto-temporal regions; adolescent; analysis of variance; cerebral cortex; child; cognitive therapy; double-blind method; dyslexia; female; functional laterality; humans; male; transcranial direct current stimulation; treatment outcome; reading; medicine (all); neurology; developmental neuroscience; neurology (clinical)03 medical and health sciencesSettore MED/39 - NEUROPSICHIATRIA INFANTILEDouble-Blind Methodmental disordersmedicineHumans0501 psychology and cognitive sciencesmedicine (all)parieto-temporal regionAnalysis of VarianceCognitive Behavioral TherapyneurologyDyslexiamedicine.diseaseWord lists by frequencydevelopmental neuroscienceReadingBrain stimulationcognitive therapy030217 neurology & neurosurgeryRestorative neurology and neuroscience
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Prader–Willi Syndrome with Angelman Syndrome in the Offspring

2021

We report the second case, to the best of our knowledge, of a mother with Prader–Willi syndrome (PWS) who gave birth to a daughter with Angelman syndrome (AS). The menarche occurred when she was 16, and the following menstrual cycles were irregular, but she never took sexual hormone replacement therapy. At the age of 26, our patient with PWS became pregnant. The diagnosis was confirmed by molecular genetic testing that revealed a ~5.7 Mb deletion in the 15q11.1–15q13 region on the paternal allele in the mother with PWS and the maternal one in the daughter with AS, respectively. Both the mother with PWS and the daughter with AS showed peculiar clinical and genetic features of the two syndrom…

Medicine (General)congenital hereditary and neonatal diseases and abnormalitiesPediatricsmedicine.medical_specialtyPrader–Willi syndromeOffspringmedia_common.quotation_subjectCase Report030209 endocrinology & metabolismFertilityHuman sexuality03 medical and health sciencesR5-9200302 clinical medicinePregnancyAngelman syndromeHumansMedicineAllelemedia_commonfertilityDaughter030219 obstetrics & reproductive medicineoffspringbusiness.industrynutritional and metabolic diseasesGeneral Medicinemedicine.diseaseSettore MED/39 - Neuropsichiatria Infantilenervous system diseasesTransgender hormone therapyAngelman syndromeMenarcheFemaleAngelman syndrome Fertility Offspring Prader–Willi syndrome Female Fertility Humans Pregnancy Angelman Syndrome Prader-Willi SyndromebusinessPrader-Willi SyndromeMedicina
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On the Playing Field to Improve: A Goal for Autism.

2020

In recent years, there has been a renewed attention to lifestyle-based interventions in people with autism spectrum disorder. The positive effects of physical exercise programs have been well documented both in healthy people and in people with disabilities in the fields of psychological well-being, cognitive outcome and medical health. There is much less evidence about the opportunity to attempt a team-group sport for people with autism. Although researchers seem to suggest an overall positive effect, playing team sports for people with autism spectrum disorder (ASD) means dealing with difficulties in social interactions and limitations in motor functions. This narrative review aims to rep…

Medicine (General)footballTeam sportAutism Spectrum DisorderPsychological interventionFace (sociological concept)autismFootballReviewASDDevelopmental psychologyR5-920mental disordersSoccermedicineASD Autism Football Soccer SportHumansAutistic DisorderExerciseLife StyleField (Bourdieu)CognitionGeneral Medicinemedicine.diseaseSettore MED/39 - Neuropsichiatria InfantileAutism spectrum disorderAutismPsychologysportMedicina (Kaunas, Lithuania)
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Temperamental characteristics in childhood migraine without aura:A multicenter study

2013

Background: Children with migraine seem to be more anxious, sensitive, deliberate, cautious, fearful, vulnerable to frustration, tidy, and less physically enduring than comparisons. To the best our knowledge no studies about the temperamental and the characterial dimension aspects in childhood migraine was conducted. Therefore, the aim of the present study was to describe the temperamental and character aspects in a sample of children affected by migraine without aura (MoA) and their relationship with clinical aspects of MoA such as frequency, duration, and severity of attacks. Materials and methods: In our study, 486 children affected by MoA (239 male, 247 female) aged 7-12 years, (mean 10…

Migraine without auraTemperamentChildrenJTCISettore MED/39 - Neuropsichiatria Infantile
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Visual–spatial training efficacy in children affected by migraine without aura: a multicenter study

2017

Francesco Precenzano,1,* Maria Ruberto,2,* Lucia Parisi,3 Margherita Salerno,4 Agata Maltese,3 Beatrice Gallai,5 Rosa Marotta,6 Serena Marianna Lavano,7 Francesco Lavano,6 Michele Roccella3 1Clinic of Child and Adolescent Neuropsychiatry, Headache Center for Children and Adolescent. Department of Mental and Physical Health and Preventive Medicine, Università degli Studi della Campania Luigi Vanvitelli, 2Department of Medical-Surgical and Dental Specialties, Università degli Studi della Campania Luigi Vanvitelli, Naples, 3Department of Psychological, Pedagogical and Educational Sciences, 4Sciences for Mother and Child Health Promotion, University of Palermo, Palermo, 5D…

Migraine without aura; Visual–motor integration; Visual–motor training skills;medicine.medical_specialtyNeuropsychiatric Disease and TreatmentAuraMigraine without aura; Visual–motor integration; Visual–motor training skills; Psychiatry and Mental Health; Biological PsychiatryAudiologyGroup BVisual–motor training skill03 medical and health sciencesSettore M-PSI/04 - Psicologia Dello Sviluppo E Psicologia Dell'Educazione0302 clinical medicineVisual–motor integrationMedicinePsychiatryBiological PsychiatryOriginal ResearchVisual–motor training skillsbusiness.industryMean ageCognitionmedicine.diseaseSettore MED/39 - Neuropsichiatria Infantile030227 psychiatryClinical PracticeMulticenter studyMigrainePsychiatry and Mental HealthMigraine without auraPopulation studybusiness030217 neurology & neurosurgeryNeuropsychiatric Disease and Treatment
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Efficacy And Tolerability of Acetazolamide in Migraine Prophylaxis and Klinefelter Syndrome: A Case Report

2013

P390 Efficacy and Tolerability of Acetazolamide in Migraine Prophylaxis and Klinefelter Syndrome: A Case Report R. Nardello1, P. Glorioso1, M. Saladino1, M. Moscarelli1, A. Fontana1, S. Mangano1 1Dipartimento di Scienze per la Promozione della Salute e Materno Infantile ‘‘G. D’Alessandro’’, University of Palermo, Palermo, PA, Italy. Objectives: We describe an interesting case of migraine headaches with aura in a 47, XXY male Klinefelter Syndrome (KS) intreatment with Acetazolamide and resolutionof symptoms. Background: A 16-year-old boy presented to the outpatient clinic migraine headaches throbbing, onset evening that lasts for a week and is presented once a month with aura, associated wit…

Migraine AcetazolamideSettore MED/39 - Neuropsichiatria Infantile
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Motor disabilities in the Rett Syndrome

2008

Motor rettSettore MED/39 - Neuropsichiatria Infantile
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