Search results for "Infantile"

showing 10 items of 461 documents

Electroencephalographic Abnormalities in Autism Spectrum Disorder: Characteristics and Therapeutic Implications.

2020

A large body of literature reports the higher prevalence of epilepsy in subjects with Autism Spectrum Disorder (ASD) compared to the general population. Similarly, several studies report an increased rate of Subclinical Electroencephalographic Abnormalities (SEAs) in seizure-free patients with ASD rather than healthy controls, although with varying percentages. SEAs include both several epileptiform discharges and different non-epileptiform electroencephalographic abnormalities. They are more frequently associated with lower intellectual functioning, more serious dysfunctional behaviors, and they are often sign of severer forms of autism. However, SEAs clinical implications remain controver…

Malemedicine.medical_specialtyMedicine (General)Autism Spectrum Disorderautism spectrum disordersPopulationEpiphenomenonDysfunctional familyChild Behavior DisordersReviewAudiologybehavioral disciplines and activities03 medical and health sciencesEpilepsy0302 clinical medicineBorderline intellectual functioningR5-920mental disordersmedicineHumansCognitive DysfunctioneducationChildSubclinical infectioneducation.field_of_studyEpilepsyEvidence-Based MedicineEpileptogenic abnormalitiebusiness.industryepileptogenic abnormalitiesElectroencephalographyGeneral Medicineelectroencephalogrammedicine.diseaseSettore MED/39 - Neuropsichiatria Infantile030227 psychiatryAutism spectrum disorderAutismAnticonvulsantsFemaleAutism spectrum disorders Electroencephalogram Epilepsy Epileptogenic abnormalities Non-epileptiform abnormalitiesbusinessnon-epileptiform abnormalities030217 neurology & neurosurgeryMedicina (Kaunas, Lithuania)
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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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Complications of trans-anastomotic externalised stents in open pyeloplasty: influence of the method of placement, the duration of stenting, and the a…

2010

To assess the influence of the method for stent placement, the duration of stenting, and the presence of bladder drainage on the complication rate of open pyeloplasty. Patients and methods: Complications were, retrospectively, compared in 228 consecutive open pyeloplasties performed at institution A using a trans-pyelostomic 6-Fr splint/stent for 5 days and no bladder drainage, and 150 consecutive open pyeloplasties performed at institution B using a trans-nephrostomic 6-Fr splint/stent for 9 days plus bladder drainage. Results: Median age at surgery was comparable between groups. The overall complication rate was 13% and was comparable at the two institutions, but for the presence of perio…

Malemedicine.medical_specialtyPyeloplastypyeloplastyTime FactorscomplicationsAdolescentmedicine.medical_treatmentAnastomosisOpen pyeloplastyYoung AdultPostoperative ComplicationsPediatric surgeryStentPrevalencemedicineHumansComplication ratecardiovascular diseasesChildHydronephrosisBladder drainageRetrospective Studiesbusiness.industrySettore MED/20 - Chirurgia Pediatrica E InfantileAnastomosis SurgicalInfantStentEquipment DesignGeneral Medicineequipment and suppliesmedicine.diseaseSurgeryTreatment Outcomesurgical procedures operativeItalyChild PreschoolPediatrics Perinatology and Child HealthDrainageUrologic Surgical ProceduresFemaleKidney DiseasesStentsSurgeryUrinary CatheterizationbusinessPediatric Surgery International
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Gastroesophageal reflux in patients treated for congenital diaphragmatic hernia: short- and long-term evaluation with multichannel intraluminal imped…

2013

The incidence of GER, related symptoms and complications in patients treated for congenital diaphragmatic hernia (CDH) are poorly defined. The aim was to evaluate incidence and development of GER in children treated for CDH in a short- and long-term follow-up period, identifying potential risk factors of morbidity. Thirty-six patients were evaluated with pH-MII at a median age of 6 months (T1) and re-evaluated with pH-MII and endoscopy at a median age of 5 years (T2). The incidence of reflux was 83 % in T1 and 61 % in T2; the incidence of symptoms was 62 % in T1 and 38 % in T2. In both groups the reflux was mainly non-acidic. Patch, intrathoracic stomach and esophageal dysmotility were risk…

Malemedicine.medical_specialtyTime FactorsCongenital diaphragmatic hernia Gastroesophageal reflux disease Esophageal dysmotility Multichannel intraluminal impedance Endoscopic esophagitisDiaphragmatic breathingAsymptomaticGastroenterologyEsophagusInternal medicinemedicineElectric ImpedanceHumansHerniaRisk factorHerniorrhaphyRetrospective StudiesHernia Diaphragmaticbusiness.industryIncidence (epidemiology)IncidenceSettore MED/20 - Chirurgia Pediatrica E InfantileRefluxCongenital diaphragmatic herniaInfantGeneral MedicineHydrogen-Ion Concentrationmedicine.diseaseSurgeryItalyPediatrics Perinatology and Child HealthGastroesophageal RefluxSurgeryFemaleEsophagoscopymedicine.symptombusinessHernias Diaphragmatic CongenitalEsophagitisFollow-Up StudiesPediatric surgery international
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Failed hypospadias in paediatric patients

2013

Failed hypospadias refers to any hypospadias repair that leads to complications or causes patient dissatisfaction. The complication rate after hypospadias repairs ranges from 5-70%, but the actual incidence of failed hypospadias is unknown as complications can become apparent many years after surgery and series with lifelong follow-up data do not exist. Moreover, little is known about uncomplicated repairs that fail in terms of patient satisfaction. Risk factors for complications include factors related to the hypospadias (severity of the condition and characteristics of the urethral plate), the patient (age at surgery, endocrine environment, and wound healing impairment), the surgeon (tech…

Malemedicine.medical_specialtyUrethral strictureUrologyFistulaUrethroplastymedicine.medical_treatmentcomplicationDehiscencehypospadias; pediatrics; complications;Postoperative ComplicationsmedicineHumansTreatment FailureChildGlansHypospadiasbusiness.industrySettore MED/20 - Chirurgia Pediatrica E Infantilehypospadiamedicine.diseaseMeatal stenosisSurgerypediatricmedicine.anatomical_structureUrethraHypospadiasHypospadiaPostoperative ComplicationbusinessChild; Humans; Hypospadias; Male; Postoperative Complications; Treatment Failure; UrologyHumanNature Reviews Urology
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Management of hydrocele in adolescent patients

2010

Hydrocele is defined as an abnormal collection of serous fluid in the potential space between the parietal and visceral layers of the tunica vaginalis. In the majority of affected adolescents, hydrocele is acquired and is idiopathic in origin. The pathogenesis of idiopathic hydrocele is thought to be an imbalance in the normal process of fluid production and reabsorption. The diagnosis is usually clinical. Taking a thorough history is essential to rule out any fluctuation in size, which is an indication of a patent processus vaginalis. Scrotal ultrasonography is mandatory in nonpalpable testicles to rule out a subtending testicular solid mass requiring inguinal exploration. Otherwise, open …

Malemedicine.medical_specialtyUrologic Surgical Procedures MaleUrologyUrologic Surgical ProcedurehydroceleHydroceleMedicineHumanshydrocele; adolescent; surgical therapy;business.industryStandard treatmentTunica vaginalisSettore MED/20 - Chirurgia Pediatrica E InfantileAge FactorsPatent processus vaginalisDisease ManagementSolid massmedicine.diseaseSurgeryTesticular HydroceleDissectionSerous fluidmedicine.anatomical_structureadolescentsurgical therapybusiness
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The Fate of Nephrons in Congenital Obstructive Nephropathy: Adult Recovery is Limited by Nephron Number Despite Early Release of Obstruction

2015

Urinary tract obstruction and reduced nephron number often occur together as a result of maldevelopment of the kidneys and the urinary tract. We determined the role of nephron number on adaptation of the remaining nephrons of mice subjected to neonatal partial unilateral ureteral obstruction followed through adulthood.Wild-type and Os/+ mice (the latter with 50% fewer nephrons) underwent sham operation or partial unilateral ureteral obstruction in the first 2 days of life. Additional mice underwent release of unilateral ureteral obstruction at 7 days. All kidneys were harvested at 3 weeks (weaning) or 6 weeks (adulthood). Glomerular number and area, glomerulotubular junction integrity, prox…

Malemedicine.medical_specialtyUrologyUrinary systemKidney GlomerulusUrologygrowth and developmentCell CountNephronurologic and male genital diseasesArticleureteral obstructionMiceMaldevelopmentInternal medicinemedicineAnimalsWeaningdisease progression; growth and development; nephrons; ureteral obstructionRenal InsufficiencyCell ProliferationKidneyDisease progressionurogenital systembusiness.industrySettore MED/20 - Chirurgia Pediatrica E InfantileNephronsKidney Glomerulusmedicine.diseasenephronObstructive NephropathyDisease Models Animalmedicine.anatomical_structureEndocrinologyAnimals NewbornFemaleUrinary tract obstructionbusiness
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Fibrosarcoma in pediatric patients: Results of the Italian Cooperative Group Studies (1979-1995)

2001

Background and Objectives Fibrosarcoma is a rare soft tissue sarcoma (STS) that has two peaks of incidence in pediatric patients: one in infants and young childern (infantile fibrosarcoma), another in older children (“adult type” fibrosarcoma). The purpose of this study was to describe the clinical features and the treatment results in patients affected by fibrosarcoma enrolled in two consecutive studies run by the STS-Italian Cooperative Group (ICG) between 1979 and 1995. Patients and Methods Twenty-five evaluable patients were grouped according the intergroup rhabdomyosarcoma staging (IRS) system: 12 Gr I, 5 Gr II, 8 Gr III. The cut-off point between the two forms was considered the age o…

Malemedicine.medical_specialtyinfantile fibrosarcomaAdolescentmedicine.medical_treatmentSoft Tissue NeoplasmsSettore MED/38 - Pediatria Generale E SpecialisticamedicineHumansFibrosarcomaRhabdomyosarcomaChildSurvival analysisfibrosarcoma; infantile fibrosarcoma; soft tissue sarcomabusiness.industrySoft tissue sarcomaSettore MED/20 - Chirurgia Pediatrica E InfantileAge FactorsInfantRadiotherapy DosageSarcomaGeneral Medicinemedicine.diseaseCombined Modality TherapySurvival AnalysisSurgeryRadiation therapyTreatment OutcomeOncologyChild Preschoolsoft tissue sarcomaSurgeryFemalefibrosarcomaSarcomaInfantile FibrosarcomabusinessProgressive disease
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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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