Search results for "Fetus"

showing 10 items of 293 documents

Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approach.

1995

Based on two unrelated index patients afflicted with INCL, fetal chorion tissues were studied from subsequent pregnancies of the two respective mothers resulting in the prenatal diagnosis of INCL in two of the three pregnancies. Documentation of INCL was based on electron microscopy and DNA studies of the biopsied chorion tissue, later confirmed in the two affected fetuses after termination of their pregnancies by demonstrating INCL-specific lipopigments in post-mortem tissues, in the liver of both aborted fetuses and, additionally, in spleen and skeletal muscle of one of the affected fetuses. The autolysis of the aborted tissues, however, precluded a systematic documentation of all affecte…

MalePathologymedicine.medical_specialtyCell typeBiopsyInfantile neuronal ceroid lipofuscinosisSpleenPrenatal diagnosisBiologyConsanguinityDevelopmental NeuroscienceNeuronal Ceroid-LipofuscinosesPregnancyPrenatal DiagnosisBiopsymedicineHumansreproductive and urinary physiologyFetusmedicine.diagnostic_testAborted FetusSkeletal muscleInfantAbortion InducedGeneral MedicineChorionDNAmedicine.diseasePedigreeMicroscopy Electronmedicine.anatomical_structureLiverembryonic structuresPediatrics Perinatology and Child HealthFemaleNeurology (clinical)Braindevelopment
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Probable exclusion of juvenile neuronal ceroid lipofuscinosis in a fetus at risk: an interim report.

1989

In a family with two children affected by juvenile neuronal ceroid lipofuscinosis (JNCL) an attempt was made at the prenatal diagnosis of the disorder. The following tissues from the fetus at risk were investigated by electron microscopy and were found to be free of fingerprint profiles and curvilinear bodies, typical for JNCL: uncultivated amniotic fluid cells, lymphocytes isolated from fetal blood, and fetal skin biopsy specimens. The child was born at the 34th week of gestation and was clinically normal at the age of 15 months. Postnatally, lymphocytes (isolated at the age of 6 and 15 months) and skin tissue (taken at the age of 15 months) were found to be morphologically normal. It is h…

MalePathologymedicine.medical_specialtyFetus at riskBiopsyPrenatal diagnosisBiologyNeuronal Ceroid-LipofuscinosesPregnancyRisk FactorsBiopsymedicineHumansGenetics (clinical)SkinPregnancyFetusmedicine.diagnostic_testObstetrics and GynecologyInfantmedicine.diseaseFetal DiseasesAmniocentesisAmniocentesisGestationNeuronal ceroid lipofuscinosisFemalePrenatal diagnosis
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Customized and non-customized live-born birth-weight curves of single and uncomplicated pregnancies from the Burgundy perinatal network. Part I – met…

2017

International audience; Objectives: To establish non-customized and customized birth-weight curves of single and uncomplicated pregnancies according to gestational age.Materials and methods: We used data for 64,173 mother-infants pairs from the Burgundy perinatal network database (France) over the period 2005-2013. A validated procedure was used to link mothers with their newborns, and maternal and fetal pathologies likely to affect birth weight were excluded. Multiple regression analysis with covariate selection was used to build a customized growth curve with maternal and fetal parameters.Results: Using this methodology, three different curves were generated: an unadjusted curve for birth…

MalePediatrics[SDV]Life Sciences [q-bio]BirthweightIntrauterine growth restrictionCommunity NetworksPerinatal networkFetal Development0302 clinical medicinePregnancyBirth WeightMedicine030212 general & internal medicineGrowth ChartsPrecision Medicineeducation.field_of_studyFetal Growth Retardation030219 obstetrics & reproductive medicineObstetricsObstetrics and GynecologyGestational ageSmall for gestational ageWeight curvesFetal WeightInfant Small for Gestational AgeGestationFemaleFranceLive BirthAdultmedicine.medical_specialtyBirth weightPopulationIntrauterine growth restrictionHospitals MaternityUltrasonography PrenatalYoung Adult03 medical and health sciencesPredictive Value of TestsCovariateHumanseducationFetus[ SDV ] Life Sciences [q-bio]business.industryInfant Newbornmedicine.diseaseReproductive MedicineCustomized chartsSmall for gestational agebusinessJournal of Gynecology Obstetrics and Human Reproduction
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Early-life weight gain, prematurity, and asthma development.

2014

Early childhood asthma is a clinical syndrome, the development and clinical manifestations of which result from a complex interplay among airway anatomy, physiology, and inflammation. Although multiple phenotypes of early childhood wheezing and asthma have been described, the mechanisms that promote and differentiate these phenotypes remain poorly understood. Over the past decade, substantial understanding has emerged as to the early-life factors that influence childhood asthma development. One area of great interest has been the relationships between patterns of fetal and infant growth, subsequent wheezing, and asthma. Although several studies strongly suggest that intrauterine growth patt…

MalePediatricsmedicine.medical_specialtyAllergyBirth weightImmunologyBMI Body mass indexWeight GainAsthma and Lower Airway Diseasechildrencohort studiesWheezemedicineImmunology and AllergyBirth WeightHumansEarly childhoodlow birth weightSDS Standard deviation scoresAsthmaFetusinfant growthISAAC International Study on Asthma and Allergy in Childhoodbusiness.industrywheezingGestational ageasthmamedicine.diseasepOR Pooled odds ratioPremature BirthFemaleepidemiologymedicine.symptombusinessBody mass indexWeight gainOR Odds ratioThe Journal of allergy and clinical immunology
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Delayed vs Immediate Cord Clamping Changes Oxygen Saturation and Heart Rate Patterns in the First Minutes after Birth

2020

Objective To build arterial oxygen saturation (SpO2) and heart rate (HR) percentiles for the first 10 minutes after birth in term infants born after an uneventful gestation, vaginal delivery, and delayed cord clamping (DCC) for ≥60 seconds, and to compare our results with previous ones constructed after immediate cord clamping. Study design Preductal SpO2, HR, and timing of DCC immediately after complete fetal body expulsion were recorded. The pulse-oximeter was adjusted in the right wrist/hand and set at maximal intensity and measurements performed every 2 seconds. Results A total of 282 term newborn infants were included. The definitive data set comprised of 70 257 SpO2 and 79 746 HR meas…

MaleTime FactorsUmbilical cordUmbilical CordConstriction03 medical and health sciences0302 clinical medicineHeart Rate030225 pediatricsHeart ratemedicineHumansOximetry030212 general & internal medicineFetusbusiness.industryVaginal deliveryfungiInfant NewbornConstrictionIntensity (physics)Oxygenmedicine.anatomical_structureAnesthesiaPediatrics Perinatology and Child HealthBreathingGestationFemalebusinessThe Journal of Pediatrics
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Report on Intrauterine Drug Exposure During Second Trimester of Pregnancy in a Heroin-Associated Death

1999

A 17-year-old girl was found dead in a public toilet with fresh needle puncture marks. She was 18-20 weeks pregnant with a male fetus. Drug screening of her blood and urine indicated recent heroin use. Chronic drug use was confirmed by hair analysis. Amniotic fluid as well as fetal and maternal tissues and body fluids were analyzed by GC/MS and HPLC. All the fetal specimens were investigated, and the following levels of drugs were found: 6-monoacetyl-morphine (blood: 152 ng/g; amniotic fluid: 128 ng/g; brain: 140 ng/g; lung: 110 ng/g; liver: 2 ng/g; kidney: 40 ng/g), morphine (blood: 1360 ng/g; amniotic fluid: 604 ng/g; brain: 710 ng/g; lung: 1030 ng/g; liver: 2060 ng/g; kidney: 1100 ng/g),…

Malemedicine.medical_specialtyAmniotic fluidAdolescentUrineGas Chromatography-Mass SpectrometryFatal OutcomeFetusPharmacokineticsPregnancyInternal medicinemedicineHumansTissue DistributionPharmacology (medical)Maternal-Fetal ExchangePharmacologyMorphine DerivativesKidneyFetusCodeinebusiness.industryHair analysisAmniotic FluidOpioid-Related DisordersBody FluidsHeroinPregnancy Complicationsmedicine.anatomical_structureFetal circulationEndocrinologyPregnancy Trimester SecondGestationFemaleAutopsybusinessHairTherapeutic Drug Monitoring
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Decreased cell proliferation and higher oxidative stress in fibroblasts from Down Syndrome fetuses. Preliminary study

2013

Abstract Down Syndrome is the most common chromosomal disease and is also known for its decreased incidence of solid tumors and its progeroid phenotype. Cellular and systemic oxidative stress has been considered as one of the Down Syndrome phenotype causes. We correlated, in a preliminary study, the fibroblast proliferation rate and different cell proliferation key regulators, like Rcan1 and the telomere length from Down Syndrome fetuses, with their oxidative stress profile and the Ribonucleic acid and protein expression of the main antioxidant enzymes together with their activity. Increased oxidized glutathione/glutathione ratio and high peroxide production were found in our cell model. Th…

Malemedicine.medical_specialtyAntioxidantmedicine.medical_treatmentPrimary Cell CultureSuperoxide dismutasemedicine.disease_causeSuperoxide dismutasechemistry.chemical_compoundFetusSuperoxide Dismutase-1ThioredoxinsInternal medicineGlutaredoxinmedicineHumansThioredoxinMolecular BiologyGlutaredoxinsCell ProliferationSkinchemistry.chemical_classificationReactive oxygen speciesGlutathione PeroxidaseTelomere lengthbiologyGlutathione peroxidaseTelomere HomeostasisGlutathioneRcan1FibroblastsTelomereCatalaseGlutathioneProgeroidOxidative StressEndocrinologychemistryBiochemistryGene Expression Regulationbiology.proteinMolecular MedicineFemaleThioredoxinDown SyndromeOxidative stressSignal TransductionBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
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Perinatal xenohormone exposure impacts sweet preference and submandibular development in male rats.

2013

Objective To determine the effect of perinatal exposure to low doses of genistein and/or vinclozolin on submandibular salivary gland (SSG) development in juvenile and adult male rats and to establish a link with sweet preference. Material and Methods Female rats received orally (1 mg kg−1 body weight/day) genistein and vinclozolin, alone or in combination, from the first gestational day up to weaning. Sweet preference was assessed at weaning and in adulthood in male offspring; submandibular glands were then collected to study the morphogenesis and mRNA expression of steroid receptors, growth factors and taste related proteins. Results Exposure to genistein and/or vinclozolin resulted in a h…

Malemedicine.medical_specialtyOffspringsalivary glandsSubmandibular Glandendocrine disruptor mixtureGenisteinPhytoestrogensBiology03 medical and health scienceschemistry.chemical_compoundFood Preferences0302 clinical medicineFetusSaccharinstomatognathic systemInternal medicineProgesterone receptormedicineWeaningEndocrine systemAnimalsVinclozolinRats WistarGeneral DentistryOxazoles030304 developmental biology0303 health sciencesPerinatal Exposuregrowth factorAndrogen AntagonistsSex hormone receptorGenisteinRatsEndocrinologyOtorhinolaryngologychemistryAnimals NewbornTastephytoestrogen[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition030217 neurology & neurosurgeryOral diseases
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A premature infant with Costello syndrome due to a rare G13C HRAS mutation.

2009

Costello syndrome is caused by mutations in the HRAS proto-oncogene whose clinical features in the first year of life include fetal and neonatal macrosomia with subsequent growth impairment due to severe feeding difficulties. We report on a premature male with Costello syndrome due to a rare G13C HRAS mutation and describe his clinical features and evolution during the first year of life. The diagnosis of Costello syndrome may be difficult at birth, especially in very preterm infants in whom feeding difficulties, reduced subcutaneous adipose tissue and failure to thrive are also part of their typical presentation.

Malemedicine.medical_specialtyPediatricsDevelopmental DisabilitiesProto-Oncogene MasprematureSettore MED/38 - Pediatria Generale E SpecialisticaCostello syndromePregnancyInternal medicineIntellectual DisabilityGeneticsmedicineHumansHRASGenetics (clinical)FetusPregnancybusiness.industryInfant NewbornNucleic acid amplification techniqueDNASyndromemedicine.diseaseEndocrinologyGenes rasSettore MED/03 - Genetica MedicaFailure to thriveMutation (genetic algorithm)MutationFemalePresentation (obstetrics)medicine.symptombusinessNucleic Acid Amplification TechniquesInfant PrematureAmerican journal of medical genetics. Part A
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Type V aplasia cutis congenita in a preterm newborn successfully resolved

2020

Aplasia cutis congenita (ACC) associated with fetus papyraceus is a rare subtype of aplasia cutis categorized as type V in Frieden's classification. It is characterized by stellate lesions in a symmetrical distribution over the trunk and proximal extremities. Conservative treatment is recommended, but there is not a well-defined therapeutic protocol. We report the case of a type V ACC in a preterm male newborn with lesions on the trunk and scalp successfully treated with topical 1% silver sulfadiazine and petrolatum gauze with an excellent evolution. This case associates a severe affectation of the scalp which represents a rare variant of type V ACC.

Malemedicine.medical_specialtyPetrolatumDermatologySilver sulfadiazineAplasia cutis congenita030207 dermatology & venereal diseases03 medical and health sciences0302 clinical medicineEctodermal DysplasiamedicineHumansFetus papyraceusScalpbusiness.industryInfant NewbornTorsoGeneral MedicineDermatologiaDermatologyTrunkBandagesConservative treatmentstomatognathic diseasesmedicine.anatomical_structure030220 oncology & carcinogenesisScalpmedicine.symptombusinessAplasia cutismedicine.drug
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