Search results for "Anomalies"

showing 10 items of 97 documents

Prevalence of anatomical variants and coronary anomalies in 543 consecutive patients studied with 64-slice CT coronary angiography

2008

The aim of our study was to assess the prevalence of variants and anomalies of the coronary artery tree in patients who underwent 64-slice computed tomography coronary angiography (CT-CA) for suspected or known coronary artery disease. A total of 543 patients (389 male, mean age 60.5 +/- 10.9) were reviewed for coronary artery variants and anomalies including post-processing tools. The majority of segments were identified according to the American Heart Association scheme. The coronary dominance pattern results were: right, 86.6%; left, 9.2%; balanced, 4.2%. The left main coronary artery had a mean length of 112 +/- 55 mm. The intermediate branch was present in the 21.9%. A variable number …

Coronary angiographyAdultMalemedicine.medical_specialty64 slice ctCoronary Vessel AnomaliesContrast MediaCoronary Angiographymultislice computed tomographyIopamidolCoronary circulationInternal medicineCoronary CirculationCoronary artery circulation Multislice computed tomography Anatomical variants AnomaliesmedicinePrevalenceHumansRadiology Nuclear Medicine and imagingNeuroradiologyAgedAged 80 and overmedicine.diagnostic_testbusiness.industryInterventional radiologyGeneral MedicineMiddle Agedanatomical variantsIopamidolCoronary arteriesmedicine.anatomical_structurecoronary artery circulation; multislice computed tomography; anatomical variants; anomaliesRadiology Nuclear Medicine and imagingCardiologycoronary artery circulationRadiographic Image Interpretation Computer-AssistedanomaliesFemaleRadiologybusinessTomography X-Ray ComputedSettore MED/36 - Diagnostica Per Immagini E RadioterapiaCardiacmedicine.drugArteryEuropean Radiology
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Right coronary artery arising from pulmonary trunk: assessment with conventional coronary angiography and multislice computed tomography coronary ang…

2009

We present a case of a 59-year-old man who was admitted to the hospital because of atypical chest pain and dyspnea. Conventional coronary angiography showed an anomalous origin of the right coronary artery from the pulmonary trunk. The patient underwent multislice computed tomography in order to clarify the origin and course of the anomalous vessel. The aim of this report is to emphasize the role of multislice computed tomography as an accurate noninvasive imaging tool in the evaluation of coronary artery anomalies.

Coronary angiographyRight coronary arteryMalemedicine.medical_specialtyCoronary Vessel AnomaliesContrast MediaPulmonary ArteryCoronary AngiographyIopamidolAngina PectorisPredictive Value of Testsmedicine.arterymedicineHumansPulmonary Trunkbusiness.industryGeneral MedicineMultislice computed tomographyMiddle AgedIopamidolmedicine.anatomical_structureDyspneaRight coronary arteryPredictive value of testsPulmonary arteryRadiologyCardiology and Cardiovascular MedicinebusinessTomography X-Ray ComputedArterymedicine.drugJournal of cardiovascular medicine (Hagerstown, Md.)
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Anatomical variants and anomalies of the coronary tree studied with MDCT coronary angiography

2010

Le anomalie delle arterie coronariche sono presenti alla nascita nella maggior parte dei casi asintomatiche ma possono manifestarsi con sintomatologia severa quale angina pectoris o addirittura l’arresto cardiaco. L’angiografia coronarica mediante tomografia computerizzata multistrato (TCMS) permette, tramite ricostruzioni multiplanari secondo piani curvilinei e riformattazioni 3D, la visualizzazione dell’albero coronarico e delle sue varianti ed anomalie in maniera non invasiva, fornendo migliore e più accurata alternativa alla angiografia coronarica (AC). Lo scopo di questo pictorial consiste nella descrizione mediante immagini TCMS con ricostruzioni multiplanari e 3D delle principali var…

Coronary angiographymedicine.medical_specialtyFistulaCoronary anomaliesCoronary Vessel AnomaliesFistulaAsymptomaticAnginaImaging Three-DimensionalHumansMedicineRadiology Nuclear Medicine and imagingcardiovascular diseasesNeuroradiologyCoronary variantsmedicine.diagnostic_testbusiness.industryMDCTInterventional radiologyGeneral Medicinemedicine.diseaseMiocardial bridgingRadiographic Image EnhancementCoronary arteriesmedicine.anatomical_structurecardiovascular systemTomographyRadiologymedicine.symptomcoronary angiographyTomography X-Ray ComputedbusinessSettore MED/36 - Diagnostica Per Immagini E RadioterapiaMDCT; coronary angiography; Coronary anomalies; Coronary variants; Miocardial bridging; FistulaMDCT coronary angiography Coronary anomalies Coronary variants Miocardial bridging Fistula
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Fraser syndrome: epidemiological study in a European population

2013

Fraser syndrome is a rare autosomal recessive disorder characterized by cryptophthalmos, cutaneous syndactyly, laryngeal, and urogenital malformations. We present a population-based epidemiological study using data provided by the European Surveillance of Congenital Anomalies (EUROCAT) network of birth defect registries. Between January 1990 and December 2008, we identified 26 cases of Fraser syndrome in the monitored population of 12, 886, 464 births (minimal estimated prevalence of 0.20 per 100, 000 or 1:495, 633 births). Most cases (18/26 ; 69%) were registered in the western part of Europe, where the mean prevalence is 1 in 230, 695 births, compared to the prevalence 1 in 1, 091, 175 fo…

CryptophthalmosMalemedicine.medical_specialtyEpidemiologyAnorectal anomaliesPopulationprevalencePrevalencePrenatal diagnosisinduced abortionCongenital abnormalitiesPregnancyInduced abortionGeneticsPrevalenceMedicineHumansCRITERIASyndactylyRegistriesPRENATAL-DIAGNOSISeducationFraser syndromeRenal agenesisGenetics (clinical)education.field_of_studycongenital abnormalitiesprenatal diagnosisFraser syndrome; epidemiology; prevalence; congenital abnormalities; prenatal diagnosis; induced abortionbusiness.industryObstetricsMUTATIONSInfant Newbornmedicine.diseaseBilateral Renal AgenesisEuropeEpidemiologic StudiesCRYPTOPHTHALMOSFemaleepidemiologyFraser syndromebusiness
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Fragile X-syndrome: literature review and report of two cases

2009

Fragile X-syndrome is caused by a mutation in chromosome X. It is one of the most frequent causes of learning disability. The most frequent manifestations of fragile X-syndrome are learning disability, different orofacial morphological alterations and an increase in testicle size. The disease is associated with cardiac malformations, joint hyperextension and behavioural alterations. We present two male patients aged 17 and 10 years, treated in our Service due to severe gingivitis. Both showed the typical facial and dental characteristics of the syndrome. In addition, we detected the presence of root anomalies such as taurodontism and root bifurcation, which had not been associated with frag…

Deficiència mentalAnomalies cromosòmiquesMental deficiencyDental abnormalitiesChromosome abnormalitiesMalalties hereditàriesMalformacions dentalsUNESCO:CIENCIAS MÉDICASGenetic diseases
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A rare case of congenital absence of permanent canines associated with other dental anomalies

2011

Agenesis of permanent canines is a rare condition and that of both maxillary and mandibular permanent canines is extremely rare. Reports of such cases are very scarce in the literature. It may occur either isolated or in association with other dental anomalies. This paper reports an unusual case of agenesis of both the maxillary permanent canines and mandibular right permanent canine occurring in association with congenitally missing mandibular permanent central incisors and microdontic maxillary lateral incisors in a 10 year-old Indian male.

Dental anomaliesUnusual casebusiness.industryDentistryOdontologíamedicine.disease:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludstomatognathic diseasesstomatognathic systemAgenesisUNESCO::CIENCIAS MÉDICASRare caseMedicineMaxillary central incisorbusinessGeneral Dentistry
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Odontomas are associated with impacted permanent teeth in orthodontic patients

2019

Background Odontomas are the most frequent odontogenic tumors in the oral cavity and can result in failure of eruption of permanent teeth or be associated with impacted teeth. Material and Methods The present study evaluated the prevalence of complex and compound odontomas in non-syndromic patients prior to the onset of orthodontic treatment. Panoramic radiographs of 4,267 non-syndromic patients were evaluated; 22 cases were included being 54.5% complex and 45.4% compound odontomas. Results The sample was composed predominantly by White males with mean age of 14.5 years. Complex odontomas were commonly found in the maxilla (83.3%) while compound type was mostly located on mandible (60%), pr…

Dental anomaliesbusiness.industryResearchMandibleDentistryOrthodontics030206 dentistry:CIENCIAS MÉDICAS [UNESCO]Delayed eruptionmedicine.diseaseOdontogenicstomatognathic diseases03 medical and health sciences0302 clinical medicineOdontomastomatognathic systemMaxillaUNESCO::CIENCIAS MÉDICASmedicineMaxillary central incisorbusinessGeneral Dentistry030217 neurology & neurosurgeryPermanent teethJournal of Clinical and Experimental Dentistry
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Coronary artery anomalies: incidence, pathophysiology, clinical relevance and role of diagnostic imaging

2006

Conventional coronary angiography is the gold standard for the diagnosis of coronary artery anomalies. Coronary anomalies are relatively rare findings in patients undergoing conventional coronary angiography for suspected obstructive coronary artery disease. Recently, the increasing performance of diagnostic techniques, such as electron beam tomography (EBT), magnetic resonance (MR) and, more recently, multislice computed tomography (MSCT), has enabled their application to cardiac imaging. MSCT, in particular, has a prominent role in coronary imaging due to its spatial and temporal resolution and three-dimensional capabilities. We report the incidence and pathophysiology of coronary artery …

Diagnostic Imagingmedicine.medical_specialtyCoronary Vessel AnomaliesCoronary AngiographyElectron beam tomographyMagnetic resonance angiographyCoronary artery diseaseImaging Three-DimensionalInternal medicineImage Processing Computer-AssistedmedicineMedical imagingHumansRadiology Nuclear Medicine and imagingCardiac imagingNeuroradiologymedicine.diagnostic_testbusiness.industryMagnetic resonance imagingInterventional radiologyGeneral Medicinemedicine.diseaseRadiographic Image EnhancementEchocardiographyCardiologyRadiologyTomography X-Ray ComputedbusinessMagnetic Resonance Angiography
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Automatic detection of thermal anomalies in induction motors

2021

The paper proposes a methodology based on Artificial Intelligence techniques for the automatic detection of abnormal thermal distributions in electric motors, to rapidly identify pre-faults or fault conditions. The proposed approach, applied to induction motors of different sizes, installed in waterworks plants, is based on the execution of Thermographic Non-Destructive Tests, which allow identifying abnormal operating conditions without interrupting the ordinary working conditions of the system. Thermographic images of induction motors are acquired at the installation site and with perspectives visible to the operator, which are sometimes partially obstructed. These thermographic images ar…

Electric motorthermal anomaliespre-processingArtificial neural networkComputer scienceReal-time computingconvolutional neural networkSettore ING-IND/32 - Convertitori Macchine E Azionamenti ElettriciFault (power engineering)Convolutional neural networkinfrared thermographyThermalinduction motorsAutomatic detectionImage acquisitionInduction motorOverheating (electricity)2021 IEEE International Conference on Environment and Electrical Engineering and 2021 IEEE Industrial and Commercial Power Systems Europe (EEEIC / I&CPS Europe)
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Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia

2020

Introduction Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) occurs approximately 1 in 3.500 live births representing the most common malformation of the upper digestive tract. Only half a century ago, EA/TEF was fatal among affected newborns suggesting that the steady birth prevalence might in parts be due to mutational de novo events in genes involved in foregut development. Methods To identify mutational de novo events in EA/TEF patients, we surveyed the exome of 30 case-parent trios. Identified and confirmed de novo variants were prioritized using in silico prediction tools. To investigate the embryonic role of genes harboring prioritized de novo variants we perfor…

EmbryologyCandidate geneGene ExpressionTranscriptomeMiceDatabase and Informatics MethodsMedicine and Health SciencesExomeExomeExome sequencingGenetics0303 health sciencesMultidisciplinaryComputer-Aided Drug DesignQ030305 genetics & hereditySequence analysisRGenomicsCongenital AnomaliesDNA-Binding Proteinsembryonic structuresAmino Acid AnalysisMedicineTranscriptome AnalysisTracheoesophageal FistulaResearch ArticleDrug Research and DevelopmentBioinformaticsSequence analysisScienceIn silicoBiologyResearch and Analysis Methods03 medical and health sciencesExome SequencingGeneticsCongenital DisordersAnimalsHumansddc:610Molecular Biology TechniquesEsophageal AtresiaMolecular BiologyDNA sequence analysis030304 developmental biologyHomeodomain ProteinsPharmacologyMolecular Biology Assays and Analysis TechniquesGene Expression ProfilingEmbryosDNA HelicasesBiology and Life SciencesComputational BiologyEmbryo MammalianGenome AnalysisFANCBRepressor ProteinsGene expression profilingBiological DatabasesDrug DesignMutation DatabasesMutationDevelopmental Biology
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