Search results for " DIAGNOSIS"

showing 10 items of 1378 documents

Klinische Manifestation der Lyme-Borreliose im Kindesalter

1989

We report on 4 children with different clinical manifestations of Lyme-Borreliosis. One patient presented with a stage 2 typical aseptic meningitis and 2 others with symptoms of Schonlein-Henoch purpura and rheumatic disease respectively. A further case had bilateral palsy of abducens nerve and unilateral palsy of trochlearis nerve which are described for the first time in Lyme-Borreliosis. Diagnosis was established by detection of specific antibodies to Borrelia in all patients. Differential diagnosis of these symptoms should include Lyme-Borreliosis.

Pediatricsmedicine.medical_specialtyPalsybiologybusiness.industryAseptic meningitisbacterial infections and mycosesmedicine.diseasebiology.organism_classificationPurpuraLyme diseaseBorreliaPediatrics Perinatology and Child HealthMedicineDifferential diagnosisStage (cooking)medicine.symptombusinessAbducens nerveKlinische Pädiatrie
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Neurological and Ocular Fascioliasis in Humans

2014

Fascioliasis is a food-borne parasitic disease caused by the trematode species Fasciola hepatica, distributed worldwide, and Fasciola gigantica, restricted to given regions of Africa and Asia. This disease in humans shows an increasing importance, which relies on its recent widespread emergence related to climate and global changes and also on its pathogenicity in the invasive, biliary, and advanced chronic phases in the human endemic areas, mainly of developing countries. In spite of the large neurological affection capacity of Fasciola, this important pathogenic aspect of the disease has been pronouncedly overlooked in the past decades and has not even appear within the numerous reviews o…

Pediatricsmedicine.medical_specialtyPathologybiologybusiness.industryFasciola giganticaDiseaseLiver flukemedicine.diseasebiology.organism_classificationParasitic diseasemedicineEtiologyFasciola hepaticaEosinophiliaDifferential diagnosismedicine.symptombusiness
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Chronic inflammatory demyelinating polyradiculoneuropathy: can a diagnosis be made in patients not fulfilling electrodiagnostic criteria?

2021

Background and purpose The aim was to identify the clinical and diagnostic investigations that may help to support a diagnosis of chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in patients not fulfilling the European Federation of Neurological Societies and Peripheral Nerve Society (EFNS/PNS) electrodiagnostic criteria. Methods The data from patients with a clinical diagnosis of CIDP included in a national database were retrospectively reviewed. Results In all, 535 patients with a diagnosis of CIDP were included. This diagnosis fulfilled the EFNS/PNS criteria in 468 patients (87.2%) (definite in 430, probable in 33, possible in three, while two had chronic immune sensory p…

Pediatricsmedicine.medical_specialtyResponse to therapyDatabases FactualNeural ConductionSettore MED/2603 medical and health sciences0302 clinical medicinePeripheral nerveRetrospective StudieMedicineHumansMedical historyIn patient030212 general & internal medicinePeripheral NervesRetrospective Studieschronic inflammatory demyelinating polyradiculoneuropathybusiness.industryPolyradiculoneuropathyPolyradiculopathymedicine.diseaseelectrophysiologySettore MED/26 - NEUROLOGIANeurologyPolyradiculoneuropathy Chronic Inflammatory DemyelinatingClinical diagnosisPeripheral Nervediagnostic criteriaNational databaseNeurology (clinical)chronic inflammatory demyelinating polyradiculoneuropathy; diagnostic criteria; electrophysiologybusiness030217 neurology & neurosurgeryHuman
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The cognitive profile of prion disease: a prospective clinical and imaging study

2015

Objectives Prion diseases are dementing illnesses with poorly defined neuropsychological features. This is probably because the most common form, sporadic Creutzfeldt-Jakob disease, is often rapidly progressive with pervasive cognitive decline making detailed neuropsychological investigation difficult. This study, which includes patients with inherited, acquired (iatrogenic and variant) and sporadic forms of the disease, is the only large-scale neuropsychological investigation of this patient group ever undertaken and aimed to define a neuropsychological profile of human prion diseases. Methods A tailored short cognitive examination of all of the patients (n = 81), with detailed neuropsycho…

Pediatricsmedicine.medical_specialtySettore M-PSI/02 - Psicobiologia E Psicologia Fisiologicabusiness.industryGeneral NeuroscienceNeuropsychologyCognitionDiseasePrion diseases cognitive declineBioinformaticsPRNPClinical trialBasal gangliamedicineNeurology (clinical)Differential diagnosisCognitive declinebusinessResearch ArticlesAnnals of Clinical and Translational Neurology
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Nomenclature and diagnosis of gluten-related disorders: A position statement by the Italian Association of Hospital Gastroenterologists and Endoscopi…

2017

Abstract Background “Gluten-related disorders” is a term that encompasses different diseases induced by the ingestion of gluten-containing food. Because of their incidence the scientific community has been intensively studying them. Aim To support gastroenterologists with a correct nomenclature and diagnostic approach to gluten-related disorders in adulthood. Methods The Italian Association of Hospital Gastroenterologists and Endoscopists (AIGO) commissioned a panel of experts to prepare a position statement clarifying the nomenclature and diagnosis of gluten-related disorders, focusing on those of gastroenterological interest. Each member was assigned a task and levels of evidence/recommen…

Pediatricsmedicine.medical_specialtySettore MED/09 - Medicina InternaGlutensNon-celiac gluten sensitivityWheat HypersensitivityDiseaseGastroenterologyDiagnosis DifferentialDiet Gluten-FreeHospital03 medical and health sciences0302 clinical medicineRisk FactorsFood allergyceliac disease; wheat allergy; non-celiac gluten sensitivity; gluten-related disorders; food allergyGluten-related disorderInternal medicineFood allergymedicineHumans030212 general & internal medicineRisk factorSocieties Medicalchemistry.chemical_classificationHepatologybusiness.industryRisk FactorIncidence (epidemiology)BIO/13 - BIOLOGIA APPLICATAGastroenterologynutritional and metabolic diseasesEvidence-based medicinemedicine.diseaseGlutenHospitalsWheat allergydigestive system diseasesCeliac DiseaseItalychemistry030211 gastroenterology & hepatologyDifferential diagnosisbusinessgluten-related disordersGlutenWheat allergyHuman
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Multi-spectral Pattern of Clinical Presentation and the Resultant Outcome in Central Nervous System Tuberculosis: A Single Center Study on the Ubiqui…

2020

Central nervous system (CNS) tuberculosis (TB) is a great medical masquerader having a multi-spectral pattern of clinical presentation, thereby complicating early diagnosis and appropriate management. This review article describes clinical presentation of CNS TB in a group of 47 patients, who were managed in the Nobel Medical College and Teaching Hospital in Biratnagar, Nepal during the last 2 years. We evaluated demographic profile, mode of management, and clinical outcome in these patients. The findings were that intracranial TB was present in 27 (57.5%) patients and the spinal involvement was in 20 (42.5%) patients. The most frequent presentation of the former was TB meningitis with hydr…

Pediatricsmedicine.medical_specialtyTuberculosisClinical outcomebusiness.industryDifferential diagnosimedicine.diseaseSingle CenterHydrocephalusReview articleMeningiti03 medical and health sciences0302 clinical medicineCentral nervous systemPott’s spinemedicineTuberculosis030212 general & internal medicinePresentation (obstetrics)Differential diagnosisbusinessAbscessMeningitis
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CLEFT PALATE ONLY: CURRENT CONCEPTS

2017

Cleft palate only (CPO) is one of the most common congenital malformations worldwide. The etiopathogenesis of CPO is not completely understood. Environmental factors, such as smoking, alcohol consumption, intake of drugs during pregnancy, advanced paternal age, have been demonstrated to be a risk of CPO, but conflicting results have also been published. Insufficient intake of folic acid during the pregnancy has been suggested to increase the risk for CPO. The demonstrated risk for siblings and the higher risk for monozygotic twins suggest a genetic etiopathogenesis for CPO. In some cases of CPO a prevalent mode of inheritance has been reported, but oligogenic models with reduced penetrance,…

Pediatricsmedicine.medical_specialtyWeaknessComplex diseasePrenatal diagnosisDiseaseCongenital03 medical and health sciences0302 clinical medicinemedicineGenetic epidemiologyOriginal Research Article030223 otorhinolaryngologyAerophagiaGeneral DentistryBirth defects; Cleft palate; Cleft palate only; Congenital; Genetic epidemiology; Dentistry (all)Pregnancybusiness.industrymedicine.diseasePenetranceBirth defectsCleft palate onlyCleft palate030220 oncology & carcinogenesisDentistry (all)Unintelligible speechmedicine.symptombusinessOral & Implantology
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Prevalence of cardiovascular late sequelae in long-term survivors of childhood cancer: A systematic review and meta-analysis

2017

Background Cardiovascular diseases are well-known late effects of childhood cancer and research on these late effects is a highly important emerging field. We conducted a systematic review with a meta-analysis to give an overview of the current evidence and the prevalence of late cardiovascular events. Procedure We included publications in which the study populations were children and adolescents who survived cancer. Outcome was defined as all cardiovascular clinical and subclinical endpoints or diagnoses appearing at least one year after cancer diagnosis. A systematic overview is presented for all included studies. A quantitative meta-analysis was conducted for hypertension and stroke. Res…

Pediatricsmedicine.medical_specialtybusiness.industryChildhood cancerCancer therapyCancerHematology030204 cardiovascular system & hematologymedicine.diseaseExamination method03 medical and health sciences0302 clinical medicineOncology030220 oncology & carcinogenesisMeta-analysisPediatrics Perinatology and Child HealthmedicinePhysical therapyMedical diagnosisbusinessStrokeSubclinical infectionPediatric Blood & Cancer
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Understanding Primary Ciliary Dyskinesia: Experience From a Mediterranean Diagnostic Reference Centre

2020

Background: Due to the lack of a gold standard diagnostic test, reference centres with experienced personnel and costly procedures are needed for primary ciliary dyskinesia (PCD) diagnostics. Diagnostic flowcharts always start with clinical symptoms. Therefore, the aim of this work is to define differential clinical criteria so that only patients clinically compatible with PCD are referred to reference centres. Materials and methods: 18 variables from 476 Mediterranean patients with clinically suspicious PCD were collected. After analysing cilia function and ultrastructure, 89 individuals were diagnosed with PCD and 387 had a negative diagnosis. Simple logistic regression analysis, consider…

Pediatricsmedicine.medical_specialtyclinical presentationlcsh:Medicineprimary ciliary dyskinesiaAtelectasisLogistic regressionArticlereference centres03 medical and health sciences0302 clinical medicinemedicineotorhinolaryngologic diseases030223 otorhinolaryngologystandard diagnosisPrimary ciliary dyskinesiaProductive CoughBronchiectasisbusiness.industrylcsh:RciliaGeneral MedicineGold standard (test)medicine.diseaserespiratory tract diseasesSitus inversusOtitis030228 respiratory systemmedicine.symptomStandard diagnosisbusiness
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The interval since first symptoms until diagnosis of squamous cell carcinoma in the head and neck region is still a problem in southern Brazil.

2020

Background The aim was to examine the interval since first symptoms until final diagnosis of squamous cell carcinoma (SCC) in the head and neck region in southern Brazil. Material and Methods The individuals were prospectively selected and underwent anamnesis, physical examination and interview in the first medical consultation at a Cancer Hospital from south of Brazil. Results From 488 patients who underwent clinical examination, 105 were included in the study with diagnosis of SCC. Patients average interval from first symptoms to final diagnosis was 152 days (median 86; max:1105; min: 1), the average professional interval was 108 days (median: 97; max:525; min: 1) , and the average total …

Pediatricsmedicine.medical_specialtymedicine.medical_treatmentPhysical examination03 medical and health sciences0302 clinical medicinemedicineHumansBasal cellHead and neckGeneral DentistrySecondary preventionAnamnesisOral Medicine and Pathologymedicine.diagnostic_testbusiness.industryResearchSmokingCancer030206 dentistrymedicine.disease:CIENCIAS MÉDICAS [UNESCO]OtorhinolaryngologyLate diagnosisHead and Neck NeoplasmsUNESCO::CIENCIAS MÉDICASCarcinoma Squamous CellSurgeryDenturesbusinessBrazilNeckMedicina oral, patologia oral y cirugia bucal
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