Search results for "Adolescent"

showing 10 items of 6718 documents

Developmental outcomes in adolescence of children with autism spectrum disorder without intellectual disability: A systematic review of prospective s…

2021

Individuals with Autism Spectrum Disorder (ASD) without intellectual disability (ID) represent approximately two-thirds of the ASD population. Here we focused on prospective research assessing different areas of functioning of children with ASD, without ID, until adolescence. Based on a pre-registered protocol (PROSPERO CRD42020189029), a systematic review of prospective studies (published between 01.01.2010 and 01.01.2020) was conducted. Twenty-eight studies met eligibility criteria. Findings indicated that ASD diagnosis and the Intelligence Quotient were highly stable over time across studies. Executive Functioning, Theory of Mind and Central Coherence processes tended to improve, althoug…

AdolescentAutism Spectrum DisorderCognitive NeurosciencePopulationComorbidityExecutive FunctionBehavioral NeuroscienceSocial skillsIntellectual DisabilityTheory of mindmental disordersIntellectual disabilitymedicineHumansProspective StudiesChildeducationeducation.field_of_studyIntelligence quotientmedicine.diseaseExecutive functionsNeuropsychology and Physiological PsychologyAutism spectrum disorderAutismPsychologyClinical psychologyNeuroscience & Biobehavioral Reviews
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The pandemic within the pandemic: the surge of neuropsychological disorders in Italian children during the COVID-19 era

2022

Abstract Background Quarantine and isolation measures during COVID-19 pandemic may have caused additional stress and challenged the mental health of the youth. Aim of the study is to investigate the COVID-19 pandemic impact on neuropsychological disorders (NPD) of Italian children and adolescents to provide general pediatric recommendations. Material and methods A retrospective multicenter observational study was planned by the Italian Pediatric Society (SIP) to explore the impact of COVID-19 on the access of children to pediatric Emergency Departments (pED) for the evaluation of neuropsychological symptoms, collecting the classification codes of diagnoses between March 1, 2019 and March 2,…

AdolescentCOVID19Neuropsychological disorderCOVID-19General MedicineSettore MED/38Mental HealthItalyQuarantineCOVID19; Children; Neuropsychological disordersHumansCOVID19 Children Neuropsychological disordersNeuropsychological disordersChildChildrenPandemicsHumanItalian Journal of Pediatrics
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Orbital volume and shape in Treacher Collins syndrome

2018

Orbito-palpebral reconstruction is a challenge in Treacher Collins syndrome (TCS). This study investigates orbital phenotypes in TCS using cephalometry and orbital shape analysis. Eighteen TCS and 52 control patients were included in this study, using the Dr Warehouse database. Orbital cephalometry was based on 20 landmarks, 10 planes, 16 angles, and 22 distances. Orbits were segmented. Registration-based, age-specific mean models were generated using semi-automatic segmentation, and aligned and compared using color-coded distance maps - mean absolute distance (MAD), Hausdorff distance (HD), and Dice similarity coefficient (DSC). Symmetry was assessed by mirroring and DSC computing. Central…

AdolescentCephalometryOrbits3D-cephalometryMandibulofacial Dysostosis/diagnostic imaging03 medical and health sciencesYoung Adult0302 clinical medicineImaging Three-DimensionalmedicineJournal ArticleHumansChildRetrospective Studiesbusiness.industryVolumeInfant NewbornInfant030206 dentistryAnatomymedicine.diseaseInfant newbornTreacher collinsTomography x ray computedOtorhinolaryngologyMidface030220 oncology & carcinogenesisChild PreschoolCase-Control StudiesSurgeryOral SurgerybusinessMorphometricsTomography X-Ray ComputedOrbitTreacher Collins syndromeMandibulofacial DysostosisOrbit/diagnostic imaging
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L'alessitimia come disturbo della regolazione affettiva

2014

Alexithymia is a theoretical construct concerning the ability to contact our feelings and the ability to describe them in words. It is very useful in clinical experience and also in empirical research for its operationalization and applicability possibility. After more than 40 years from its original definition, with clinical observation of patients defined “psychosomatics” according a classic definition, alexithymia has become one of the most investigated disease in the last decades. This paper aims to explore etiopathogenetic hypotheses and contemporaneous prospective within which it is possible to understand the relevance of the construct both in clinical experience and in empirical rese…

AdolescentCognitive psychologySettore M-PSI/08 - Psicologia ClinicaAffective symptomSettore MED/25 - PsichiatriaSettore MED/39 - Neuropsichiatria Infantile
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Participation in organized sports is associated with decreased likelihood of unhealthy lifestyle habits in adolescents

2018

Adolescence is a pivotal time for investing in both present and future health. Thus, it is important to identify arenas for promoting positive adolescent health behaviors and preventing negative ones. The aim of this study was to investigate the associations between organized sports participation (OSP) and a broad range of lifestyle habits in Norwegian adolescents. A comprehensive survey was completed by 13 269 junior high and high school students in southern Norway. Multivariable binary logistic regression models, adjusted for gender, age, and parental education, were used to investigate the associations between OSP and adolescent substance use, dietary habits, physical activity level, pas…

AdolescentCross-sectional studyHealth Behavior030209 endocrinology & metabolismPhysical Therapy Sports Therapy and RehabilitationNorwegianLogistic regressionOdds03 medical and health sciencesScreen time0302 clinical medicineSurveys and QuestionnairesHumansOrthopedics and Sports MedicineHealthy Lifestyle030212 general & internal medicineExerciseNorwayOdds ratiolanguage.human_languagePhysical activity levelDietlanguagePsychologySportsDemographyAdolescent healthScandinavian Journal of Medicine & Science in Sports
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Oral health of cystic fibrosis patients at a north american center: A pilot study

2019

Background The objective of this study was to describe the oral health status of Cystic Fibrosis (CF) children in a US facility. Material and Methods Twenty CF children ages 6-18 were recruited from Children’s Hospital of Wisconsin Pulmonary Clinic. Parents completed a health questionnaire. Clinical examinations checked dental caries using the dmft/DMFT index, dental hygiene using the Simplified Greene-Vermillion Index (DI-S), gingival inflammation using the Community Periodontal Index of Treatment Needs, and enamel defects using the modified Developmental Defects of Enamel Index. Results The majority (90%) brush twice a day, 65% consume sugary snacks, and 70% visit the dentist every 6 mont…

AdolescentCystic FibrosisEnamel defectsDentistryOral HealthPilot ProjectsDental CariesOral healthOral hygieneCystic fibrosis03 medical and health sciences0302 clinical medicinestomatognathic systemPrevalencemedicineHumansChildGeneral DentistryEnamel paintDMF Indexbusiness.industryResearchDMFT Index030206 dentistryDental hygiene:CIENCIAS MÉDICAS [UNESCO]Medically compromised patients in DentistryOral Hygienemedicine.diseaseUnited Statesstomatognathic diseasesOtorhinolaryngologyvisual_artUNESCO::CIENCIAS MÉDICASvisual_art.visual_art_mediumSurgeryMild gingivitisbusinessMedicina Oral Patología Oral y Cirugia Bucal
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Follow‐up of patients subjected to direct and indirect pulp capping of young permanent teeth. A retrospective study

2021

Abstract Objective A retrospective study of the success rate of direct pulp capping (DPC) and indirect pulp capping (IPC) was carried out in children between 6–14 years‐old, considering separately primary caries or caries affecting teeth with molar incisor hypomineralization (MIH). Material and methods Data were collected in a dental public health service. Following the inclusion criteria, 232 treatments were analyzed. Success was defined by the presence of a functional tooth without clinical signs or symptoms of pulpal or periapical disease. The success rate was correlated to patient gender, the affected tooth and the indication of therapy using the chi‐squared and Fisher exact test. The s…

AdolescentDentistryDental Pulp Cappingsymbols.namesakeIndirect Pulp Cappingstomatognathic systemyoung permanent teethHumansMedicineChildGeneral DentistryFisher's exact testRetrospective StudiesPermanent teethbusiness.industrySilicatesOxidesRetrospective cohort studyRK1-715Original ArticlesCalcium CompoundsPrimary cariesMolar Incisor HypomineralizationUnited StatesPulp cappingindirect pulp cappingstomatognathic diseasesTreatment OutcomeDentistrydirect pulp cappingsymbolsOriginal ArticleVital pulp therapybusinessPulp Capping and Pulpectomy AgentsDental public healthFollow-Up StudiesClinical and Experimental Dental Research
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Five-year longitudinal study of juvenile migraine headaches

2004

To evaluate the prevalence and the evolution over 5-year of juvenile migraine headaches. Sixty-four subjects selected in our 1989 epidemiological survey were included in the study. The criteria of the International Headache Society were used both in 1989 and 1994. Thirty-two out of 64 subjects (50%) had MWAO, 18 (28.1%) had MD and 14 (21.9%) had headache not classifiable (HnC). MWOA persists in 56.2%, becomes MD and HnC in 9.4% and 3.1% of cases respectively, changes to episodic tension-type headache (ETTH) in 12.5%, and remits in 18.8%. MD persists in 11.1%, becomes MWOA and HnC in 27.8% and 5.5% of cases respectively, changes to ETTH in 11.1, and remits in 44.5%. HnC persists in 14.3%, be…

AdolescentEpidemiologyMedicine (all)Migraine without auraSettore MED/26 - NeurologiaMigraineous disorder
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TCTN3 Mutations Cause Mohr-Majewski Syndrome

2012

Orofaciodigital syndromes (OFDSs) consist of a group of heterogeneous disorders characterized by abnormalities in the oral cavity, face, and digits and associated phenotypic abnormalities that lead to the delineation of 13 OFDS subtypes. Here, by a combined approach of homozygozity mapping and exome ciliary sequencing, we identified truncating TCTN3 mutations as the cause of an extreme form of OFD associated with bone dysplasia, tibial defect, cystic kidneys, and brain anomalies (OFD IV, Mohr-Majewski syndrome). Analysis of 184 individuals with various ciliopathies (OFD, Meckel, Joubert, and short rib polydactyly syndromes) led us to identify four additional truncating TCTN3 mutations in un…

AdolescentFoot Deformities CongenitalMolecular Sequence DataCiliopathiesJoubert syndromeYoung AdultFetusReportCerebellumGLI3medicineGeneticsHumansExomeHedgehog ProteinsGenetics(clinical)Sonic hedgehogChildExomeGenetics (clinical)Adaptor Proteins Signal TransducingCystic kidneyGeneticsBase SequencebiologyHomozygoteIntracellular Signaling Peptides and ProteinsMembrane ProteinsCiliary transition zoneSequence Analysis DNAOrofaciodigital Syndromesmedicine.diseaseCleft PalateCiliopathyPhenotypeMutationbiology.proteinApoptosis Regulatory ProteinsHand Deformities CongenitalSignal TransductionThe American Journal of Human Genetics
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Phenotype determining alleles in GM1 gangliosidosis patients bearing novel GLB1 mutations.

2010

Hofer D, Paul K, Fantur K, Beck M, Roubergue A, Vellodi A, Poorthuis BJ, Michelakakis H, Plecko B, Paschke E. Phenotype determining alleles in GM1 gangliosidosis patients bearing novel GLB1 mutations. GM1 gangliosidosis manifests with progressive psychomotor deterioration and dysostosis of infantile, juvenile, or adult onset, caused by alterations in the structural gene coding for lysosomal acid s-galactosidase (GLB1). In addition, allelic variants of this gene can result in Morquio B disease (MBD), a phenotype with dysostosis multiplex and entire lack of neurologic involvement. More than 100 sequence alterations in the GLB1 gene have been identified so far, but only few could be proven to …

AdolescentGenotypeNonsense mutationBlotting WesternDNA Mutational AnalysisBiologymedicine.disease_causeCell LineGenotypeChlorocebus aethiopsGeneticsmedicineMissense mutationAnimalsHumansAlleleChildGenetics (clinical)AllelesGeneticsMutationGangliosidosis GM1DysostosisInfantmedicine.diseasebeta-GalactosidasePhenotypePhenotypeGLB1Child PreschoolCOS CellsMutationClinical genetics
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