Search results for " preschool"

showing 10 items of 2099 documents

The ultra-thin bronchoscope in management of the difficult paediatric airway

1987

The use of an ultra-thin flexible fiberoptic bronchoscope with a single lumen diameter of 2.7 mm at the distal tip to assist intubation of paediatric patients with a difficult airway is reported. Two patients (ages 30 months and 18 months) with mandibular hypoplasia and one patient (three months) with the Pierre-Robin syndrome are reported. In each case two fiberoptic bronchoscopes were used. The first allowed introduction of topical local anaesthetic while the second and smaller one was used for tube placement.

medicine.medical_specialtymedicine.medical_treatmentBronchoscopyIntubation IntratrachealmedicineFiber Optic TechnologyHumansIntubationBronchoscopesPaediatric patientsPierre Robin Syndromemedicine.diagnostic_testbusiness.industryInfantGeneral MedicineTemporomandibular Joint Disordersmedicine.diseaseHypoplasiaSurgeryLumen DiameterBronchoscopesAnesthesiology and Pain MedicineChild PreschoolAnesthesiaPierre Robin syndromeFemalebusinessAirwayAnesthesia LocalCanadian Journal of Anaesthesia
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The assessment of skeletal status in young patients with Turner syndrome by 2 densitometric techniques: Phalangeal quantitative ultrasound and dual e…

2018

Background. Studies using dual energy X-ray absorptiometry (DXA) demonstrate a reduction in bone mineral density (BMD) in children and adolescents with Turner syndrome (TS). However, these studies do not take into account changes in bone size, which influence BMD in the case of short-statured patients. Phalangeal quantitative ultrasound (phQUS) measurements have shown an ability to reveal changes due to skeletal growth, aging, and bone and mineral disorders. There is limited data on bone mineral status in girls with TS assessed by 2 different techniques, i.e., DXA and phQUS. Objectives. The aim of this study was to investigate the potential negative impact of TS on bone status and to assess…

musculoskeletal diseases0301 basic medicineAdolescentmedicine.medical_treatmentMedicine (miscellaneous)Turner Syndromedual energy X-ray absorptiometry030209 endocrinology & metabolismGeneral Biochemistry Genetics and Molecular BiologyBone and Bones03 medical and health sciencesFinger PhalangesFractures Bonequantitative ultrasound0302 clinical medicineAbsorptiometry PhotonBone DensityTurner syndromeInternal MedicinemedicinePrevalenceHumansPharmacology (medical)Reference populationChildGenetics (clinical)Dual-energy X-ray absorptiometryReduction (orthopedic surgery)UltrasonographyBone mineralmedicine.diagnostic_testbusiness.industryfracturesmedicine.diseaseQuantitative ultrasound030104 developmental biologyNormal boneChild PreschoolReviews and References (medical)Lumbar spineFemalebusinessNuclear medicineAdvances in clinical and experimental medicine : official organ Wroclaw Medical University
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Does δ-sarcoglycan-associated autosomal-dominant cardiomyopathy exist?

2009

In this study we clinically and genetically characterize a consanguineous family with a homozygous novel missense mutation in the delta-sarcoglycan gene and a second delta-sarcoglycan mutation that has previously been reported to cause severe autosomal-dominant dilated cardiomyopathy. We identified a novel missense mutation in exon 6 (p.A131P) of the delta-sarcoglycan gene, which in a homozygous state leads to the clinical picture of a limb girdle muscular dystrophy. In four heterozygous carriers for the mutation, aged 3-64 years, a second sequence variant in exon 6 (p.S151A) of the delta-sarcoglycan gene was detected on the other allele. This second missense change had previously been repo…

musculoskeletal diseasesAdultCardiomyopathy DilatedMalemedicine.medical_specialtyAdolescentBiopsyDNA Mutational AnalysisCardiomyopathyMutation MissenseCompound heterozygosityArticleExonConsanguinityElectrocardiographyYoung AdultInternal medicineSarcoglycansGeneticsMedicineMissense mutationHumansMuscular dystrophyChildGenetics (clinical)Genes DominantGeneticsFamily Healthbusiness.industryMusclesMyocardiumDilated cardiomyopathyMiddle Agedmedicine.diseasePedigreeEndocrinologyEchocardiographyChild PreschoolMutation (genetic algorithm)FemalebusinessLimb-girdle muscular dystrophy
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Pfeiffer syndrome: clinical and genetic findings in five Brazilian families

2014

Pfeiffer syndrome (PS) is mainly characterized by craniosysnostosis, midface hypoplasia, great toes with partial syndactyly of the digits and broad and medially deviated thumbs. It is caused by allelic mutations in the fibroblast growth factor receptor 1 and 2 (FGFR1 and 2) genes. This study describes the clinical and genetic features of five Brazilian families affected by PS. All patients exhibited the classical phenotypes related to PS. The genetic analysis was able to detect the mutations Cys278Phe, Cys342Arg, and Val359Leu in three of these families. Two mutations were de novo, with one familial. We identified pathogenic mutations in four PS cases in five Brazilian families by PCR seque…

musculoskeletal diseasesAdultMaleAdolescentAcrocephalosyndactyliaOdontologíaBiologymedicine.disease_causeGenetic analysisExonmedicineHumansAlleleChildGeneral DentistryGeneticsMutationOral Medicine and PathologyResearchFibroblast growth factor receptor 1Crouzon syndromeAcrocephalosyndactyliaMiddle Agedmedicine.disease:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludPedigreePhenotypeOtorhinolaryngologyChild PreschoolMutationUNESCO::CIENCIAS MÉDICASPfeiffer syndromeFemaleSurgeryBrazil
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Transcriptional profiles from patients with dystrophinopathies and limb girdle muscular dystrophies as determined by qRT-PCR.

2003

Mutations in genes coding for the dystrophin-glycoprotein complex (DGC) cause inherited muscular dystrophies (MD), including Morbus Duchenne (DMD) and M. Becker (BMB) as well as limb-girdle muscular dystrophies (LGMD). New insights into the pathophysiology of the dystrophic muscle, the identification of compensatory mechanisms and additional proteins interacting with dystrophin are essential for developing new treatments. In order to define molecular mechanisms induced by lack of dystrophin and the subsequent counter-regulatory transcriptional response of degenerating muscle fibres, we have investigated the mRNA expression of 19 functionally linked genes in biopsies of patients with MD by m…

musculoskeletal diseasesAdultMaleAdolescentTranscription GeneticGene Expressionmedicine.disease_causeMuscular DystrophiesStatistics NonparametricDystrophinGenetic linkageGene expressionmedicineHumansRNA MessengerMuscular dystrophyChildGeneGlycoproteinsMutationbiologyReverse Transcriptase Polymerase Chain ReactionGene Expression ProfilingMusclesMiddle Agedmedicine.diseaseCell biologyGene expression profilingMuscular Dystrophy DuchenneNeurologyChild PreschoolMutationbiology.proteinFemaleNeurology (clinical)DystrophinNeuroscienceLimb-girdle muscular dystrophyJournal of neurology
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HLA Class II Differentiates Between Thyroid and Polyglandular Autoimmunity.

2015

The HLA class II genes are susceptibility genes for autoimmune endocrine diseases; however, scarce data are available pertaining to the determinants of genetic susceptibility to polyglandular autoimmunity (PGA). A total of 300 consecutive and unselected patients with either PGA or monoglandular autoimmune thyroid disease (AITD) and 100 healthy control subjects were genotyped for the HLA class II DRB1, -DQA1, and -DQB1 alleles. Compared to patients with AITD and controls, the HLA-DRB1*03 (pc =0.001), *04 (pc<0.001), -DQA1*03 (pc<0.001), and -DQB1*02 (pc =0.001) alleles were increased in patients with PGA. When dividing patients with Hashimoto's thyroiditis (HT) into those with PGA (PGA-HT) v…

musculoskeletal diseasesAdultMalemedicine.medical_specialtyendocrine system diseasesAdolescentEndocrinology Diabetes and MetabolismGraves' diseaseClinical BiochemistryThyroid GlandAutoimmunityImmunogeneticsHashimoto Diseasemedicine.disease_causeBiochemistryThyroiditisAutoimmunityYoung AdultEndocrinologyInternal medicineGenetic predispositionMedicineHumansHashimoto DiseaseGenetic Predisposition to DiseaseAlleleskin and connective tissue diseasesChildbusiness.industryBiochemistry (medical)ThyroidHistocompatibility Antigens Class IIInfantGeneral MedicineMiddle Agedmedicine.diseaseGraves DiseaseEndocrinologymedicine.anatomical_structureChild PreschoolImmunologyFemalebusinessHormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
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Chondrodysplasia punctata, tibia-metacarpal (MT) type.

1990

We describe 7 patients with a new form of chondrodysplasia punctata. Its principal clinical manifestations are flat midface and nose, short limbs, and otherwise normal development. Consistent radiologic manifestations in the newborn infant are discrete calcific stippling, coronal clefts of vertebral bodies, short tibiae, and shortness of the 2nd and 3rd metacarpal bones. Radiologic findings in the older child include shortness of tibiae and the 3rd and 4th metacarpals.

musculoskeletal diseasesMaleChondrodysplasia PunctataAdolescentLimb Deformities CongenitalMetacarpal bonesShort staturemedicineHumansChondrodysplasia punctataAbnormalities MultipleTibiaChildGenetics (clinical)NoseShort tibiaTibiabusiness.industryInfant NewbornInfantAnatomymusculoskeletal systemmedicine.diseaseOsteochondrodysplasiamedicine.anatomical_structureShort limbsChild PreschoolFaceFemalemedicine.symptomMetacarpusbusinessAmerican journal of medical genetics
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Mediterranean spotted fever: clinical and laboratory characteristics of 415 Sicilian children

2006

Abstract Background Mediterranean spotted fever (MSF) is an acute febrile, zoonotic disease caused by Rickettsia conorii and transmitted to humans by the brown dogtick Rhipicephalus sanguineus. Nearly four hundred cases are reported every year (mainly from June to September) on the Italian island of Sicily. The aim of the study was to analyze the clinical and laboratory characteristics of patients with MSF and the efficacy of the drugs administered. Methods Our study was carried out on 415 children with MSF, during the period January 1997 – December 2004, at the "G. Di Cristina" Children's hospital in Palermo, Sicily, Italy. On admission patients' clinical history, physical and laboratory e…

myalgiamedicine.medical_specialtyAdolescentRhipicephalus sanguineusBoutonneuse FeverAzithromycinlcsh:Infectious and parasitic diseasesInternal medicineClarithromycinmedicineHumanslcsh:RC109-216Childbiologybusiness.industryInfantmedicine.diseasebiology.organism_classificationRashAnti-Bacterial AgentsSpotted fevermediterranean spotted feverBoutonneuse feverInfectious DiseasesChild PreschoolImmunologymedicine.symptombusinessRickettsia conoriiResearch Articlemedicine.drugBMC Infectious Diseases
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Prenatal air pollution exposure and growth and cardio-metabolic risk in preschoolers

2020

Objectives: We investigated the association between outdoor air pollutants exposure in the first trimester of pregnancy, and growth and cardio-metabolic risk at four years of age, and evaluated the mediating role of birth weight. Methods: We included mother-child pairs (N = 1,724) from the Spanish INMA birth cohort established in 2003-2008. First trimester of pregnancy nitrogen dioxide (NO2) and fine particles (PM2.5) exposure levels were estimated. Height, weight, waist circumference, blood pressure, and lipids were measured at four years of age. Body mass index (BMI) trajectories from birth to four years were identified. Results: Increased PM2.5 exposure in the first trimester of pregnanc…

obesity010504 meteorology & atmospheric sciencesair pollutionprenatal exposureuse regression-models010501 environmental sciencesMalalties neonatals01 natural sciencesPregnancyInterquartile rangePrenatal exposureChildhood obesityChildlcsh:Environmental sciencesGeneral Environmental Sciencelcsh:GE1-3502. Zero hungerAir Pollutants*Childhood obesityObstetrics*Prenatal exposureChildhood growthhealthtraffic pollutionfetalPollutionMaternal ExposureChild PreschoolContaminaciómaternal smokingFemaleNeonatal diseaseschildhood obesitypregnant-womenmedicine.medical_specialtyWaistBirth weightNitrogen DioxideAir pollutioncomplex mixturesChildhood obesity*Air pollutionchildhood growthearly-childhoodmedicineHumansmediation analysis0105 earth and related environmental sciencesparticulate matterFetusPregnancybusiness.industrymedicine.disease*Particulate matterObesity*Childhood growthbusinessParticulate matterBody mass index
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Innovations in Infant Feeding: Future Challenges and Opportunities in Obesity and Cardiometabolic Disease

2020

The field of nutrition in early life, as an effective tool to prevent and treat chronic diseases, has attracted a large amount of interest over recent years. The vital roles of food products and nutrients on the body’s molecular mechanisms have been demonstrated. The knowledge of the mechanisms and the possibility of controlling them via what we eat has opened up the field of precision nutrition, which aims to set dietary strategies in order to improve health with the greatest effectiveness. However, this objective is achieved only if the genetic profile of individuals and their living conditions are also considered. The relevance of this topic is strengthened considering the importance of …

obesityPediatric ObesityInfants AlimentacióRevieweating behaviorGenetic profile0302 clinical medicineNutrigenomicsPregnancy030212 general & internal medicinePrecision MedicineChildprecision nutritionPediatriaNutrition and DieteticsNutrigenomicsCardiovascular DiseasesChild PreschoolObesitatFemaleDiet HealthyChild Nutritional Physiological Phenomenalcsh:Nutrition. Foods and food supplypediatricsAdolescentNutritional Statuslcsh:TX341-641030209 endocrinology & metabolismChildhood obesityNutrigenetics03 medical and health sciencesEnvironmental healthmedicinemicrobiotaHumansMetabolomicsGenetic Predisposition to DiseaseInfant feedingnutrigeneticsbusiness.industryInfant NewbornInfantFeeding Behaviormedicine.diseaseCardiometabolic diseaseObesitycardiometabolic risk factorsGastrointestinal MicrobiomeFood productsAvaluació del riscbusinessFood ScienceNutrients
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