Search results for " Fetal"

showing 10 items of 119 documents

Do human concepti have the potential to enter into diapause?

1999

Although there is no direct evidence as to whether human concepti have the potential to enter into diapause before implantation, the possibility that human concepti may be capable of following this developmental pathway if exposed to an appropriate environment cannot be ruled out. Direct evidence remains elusive because of the ethical restraints associated with research activities within this area of knowledge. If conceptus diapause has evolved in primates and persists at the present time despite its apparent limited or no adaptive advantage, artificial induction of diapause in humans may have clinical implications for increasing: (i) the viability of concepti after biopsy, freezing-thawing…

medicine.medical_specialtyDirect evidenceRehabilitationEmbryogenesisObstetrics and GynecologyBiologyDiapauseEmbryo MammalianAdaptation PhysiologicalCell biologyEmbryonic and Fetal DevelopmentEndometriumEndocrinologyReproductive MedicineInternal medicinemedicineConceptusHumansFemaleEmbryo ImplantationOvum implantationHuman reproduction (Oxford, England)
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Acid Ceramidase Deficiency

2015

Abstract A deficiency of the lysosomal enzyme ceramidase leads to accumulation of the sphingolipid ceramide in several organs such as skin, liver, brain and other tissues, resulting in a broad spectrum of clinical manifestations. The most common form, called Farber lipogranulomatosis, is characterized by subcutaneous skin nodules and a progressive hoarseness, in many cases also the central nervous system is affected. A lethal hydrops fetalis represents the most severe form. A ceramidase deficiency was also found in a few patients in whom neurological symptoms such as spinal muscular atrophy and myoclonus epilepsy dominated the clinical picture. In the ceramidase gene, which has been mapped …

medicine.medical_specialtyFarber diseasePathologyGenetic enhancementCentral nervous systemProgressive myoclonus epilepsySpinal muscular atrophyBiologyCeramidasemedicine.diseaseSphingolipidEndocrinologymedicine.anatomical_structureHydrops fetalisInternal medicinemedicine
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Distribution of osteonectin mRNA and protein during human embryonic and fetal development.

1992

We investigated the temporal and spatial distribution of osteonectin during human embryonic and fetal development, using in situ hybridization and immunohistochemistry. Osteonectin gene expression was generally found in cells exhibiting high rates of matrix production/proliferation. In mineralized tissue, a strong signal was obtained in osteoblasts, odontoblasts, and chondrocytes of the upper hypertrophic and proliferative zones. Chondrocytes of the mineralized zone showed no expression throughout the different stages of development. Strong osteonectin expression was found in odontoblasts of developing teeth. In addition, osteonectin mRNA and protein were detected in several non-mineralize…

medicine.medical_specialtyHistologyGene ExpressionIn situ hybridizationEmbryonic and Fetal DevelopmentFetusOsteogenesisPregnancyInternal medicineGene expressionmedicineExtracellularHumansOsteonectinRNA MessengerbiologyCartilageEmbryogenesismusculoskeletal systemEmbryo MammalianImmunohistochemistryCell biologyAbortion Spontaneousmedicine.anatomical_structureOdontoblastEndocrinologyOrgan Specificitybiology.proteinImmunohistochemistryFemaleAnatomyOsteonectinThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society
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Vitrification of zona-free rabbit expanded or hatching blastocysts: a possible model for human blastocysts.

2003

BACKGROUND: The purpose of this study was to test the effectiveness of one two-step (A) and two one-step (B1 and B2) vitrification procedures on denuded expanded or hatching rabbit blastocysts held in standard sealed plastic straws as a possible model for human blastocysts. The effect of blastocyst size was also studied on the basis of three size categories (I: diameter <200 μm; II: diameter 200-299 μm; III: diameter ≥300 μm). METHODS: Rabbit expanded or hatching blastocysts were vitrified at day 4 or 5. Before vitrification, the zona pellucida was removed using acidic phosphate buffered saline. For the two-step procedure, prior to vitrification, blastocysts were pre-equilibrated in a solut…

medicine.medical_specialtyHot TemperatureZona freeBiologyAndrologychemistry.chemical_compoundEmbryonic and Fetal DevelopmentmedicineAnimalsHumansVitrificationBlastocystZona pellucidaZona PellucidaCryopreservationTissue SurvivalDimethyl sulfoxideHatchingRehabilitationHistological TechniquesObstetrics and GynecologyEmbryoSurgerymedicine.anatomical_structureBlastocystReproductive MedicinechemistryModels AnimalFemaleRabbitsEthylene glycolHuman reproduction (Oxford, England)
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Transient expression of synaptogyrin in the ganglionic eminence of the human fetal brain

2000

Summary The ganglionic eminence (GE) representing a conspicuous bulb-like elevation of the telencephalic proliferative zone has recently been shown to be involved in the establishment of cortical connections. This study demonstrates the presence of synaptogyrin-immunoreactivity in a large number of cell bodies of the human GE between 12 and 20 weeks of gestation. From the 20 th week onwards synaptogyrin expression sharply declines. No immunoreactive structures are detectable in the 23 rd week or later. As the GE persists nearly throughout the entire fetal period these results show that its neurochemical features change distinctly in the course of development. The synaptogyrin-immunoreactive…

medicine.medical_specialtyInternal capsuleGanglionic eminenceGestational AgeNerve Tissue ProteinsBiologyEmbryonic and Fetal DevelopmentNeurochemicalPregnancyInternal medicinemedicineHumansCerebral CortexSynaptogyrinsFetal periodBrainMembrane ProteinsAbortion InducedGeneral MedicineAbortion SpontaneousEndocrinologyCell bodiesHuman fetalImmunohistochemistryFemaleAnatomySynaptogyrinDevelopmental BiologyAnnals of Anatomy - Anatomischer Anzeiger
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Patent Foramen Ovale and Thromboembolic Complications

2010

The foramen ovale, an atrial septal defect which is essential in the fetal circulation, remains patent through adulthood in approximately 25% of the general population and so it represents the most common persistent abnormality of fetal origin. Patent foramen ovale (PFO) allows interatrial right-to-left blood shunting during those periods of the cardiac cycle in which the right atrial pressure exceeds the left one. An increasing number of pathological manifestations of PFO has been recently identified; among these, paradoxical systemic embolism, refractory hypoxemia in patients with right ventricular myocardium infarction or severe pulmonary disease, orthostatic oxygen desaturation in the r…

medicine.medical_specialtyMagnetic Resonance SpectroscopyPopulationEchocardiography Three-DimensionalForamen secundumForamen Ovale PatentPersistent fetal circulationHypoxemiaPFOThromboembolismDrug DiscoverymedicineHumanseducationForamen ovale (heart)Pharmacologyeducation.field_of_studybusiness.industrySettore MED/23 - Chirurgia Cardiacamedicine.diseaseSettore MED/11 - Malattie Dell'Apparato CardiovascolareThrombosisSurgerymedicine.anatomical_structureEmbolismEchocardiographyPatent foramen ovalemedicine.symptomTomography X-Ray ComputedbusinessEchocardiography TransesophagealCurrent Pharmaceutical Design
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M-cadherin and its sisters in development of striated muscle

1999

Cadherins are calcium-dependent, transmembrane intercellular adhesion proteins with morphoregulatory functions in the development and maintenance of tissues. In the development of striated muscle, the expression and function of mainly M-, N-, and R-cadherin has been studied so far. While these three cadherins are expressed in skeletal muscle cells, of these only N-cadherin is expressed in cardiac muscle. In this review, M-, N-, and R-cadherin are discussed as important players in the terminal differentiation and possibly also in the commitment of skeletal muscle cells. Furthermore, reports are described which evaluate the essential role of N-cadherin in the formation of heart tissue.

medicine.medical_specialtyMyofilamentHistologyBiologyMuscle DevelopmentSarcomerePathology and Forensic MedicineEmbryonic and Fetal DevelopmentMiceInternal medicineMyosinmedicineAnimalsHumansMyocyteMuscle SkeletalCardiac muscleGene Expression Regulation DevelopmentalSkeletal muscleCell DifferentiationHeartCell BiologyCadherinsCell biologyEndocrinologymedicine.anatomical_structureITGA7MyofibrilCell and Tissue Research
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Long-term prediction of birth weight

1993

On the basis of the hypothesis that undisturbed individual growth in fetal life keeps a constant proportional difference with the standard population 50th percentile, birth weight can be predicted with a single sonographic exploration after the 16th week of pregnancy. Data on 135 singleton pregnancies with accurate dates and delivery at term were used. Sonography was performed between the 17th and 36th weeks of pregnancy, in every case at least 4 weeks before delivery. The observed measurements of BPD, FL, and AC were used for the prediction of their values on the day of delivery, applying the Hadlock equation for the estimation of birth weight. The mean error of birth weight predictions wa…

medicine.medical_specialtyPercentileCorrelation coefficientBirth weightUltrasonography PrenatalEmbryonic and Fetal DevelopmentPredictive Value of TestsPregnancymedicineBirth WeightHumansFalse Positive ReactionsRadiology Nuclear Medicine and imagingLongitudinal StudiesLong-term predictionFetusPregnancyRadiological and Ultrasound Technologybusiness.industryObstetricsSingletonReproducibility of ResultsGestational agemedicine.diseaseSurgeryFemalebusinessJournal of Ultrasound in Medicine
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Non‐immune hydrops fetalis was rare in Sweden during 1997‐2015, but cases were associated with complications and poor prognosis

2020

Aim: The study was designed to document the incidence of non-immune hydrops fetalis (NIHF) at birth and characterise associated outcomes and obstetric complications. Methods: Data on more than 1.9 million births were extracted from the Swedish Birth Register for 1997-2015. Pregnancies not affected by NIHF served as controls. National registers on mortality and hospitalisations provided follow-up information. Results: There were 309 cases of NIHF at birth corresponding to an incidence of 1.6 per 10 000, lower than in previous studies. NIHF was more frequent in mothers aged ≥35 years and with a history of stillbirth. Preterm delivery occurred in 77.7% in the NIHF group, including 31.7% before…

medicine.medical_specialtyPoor prognosisHydrops FetalisImmune hydrops fetalisPregnancyBirth registerHydrops fetalismedicineHumansChildAgedSwedenbusiness.industryObstetricsIncidenceIncidence (epidemiology)Infant NewbornGeneral MedicinePrognosismedicine.diseaseUnderlying diseasePediatrics Perinatology and Child HealthPremature BirthGestationPopulation studyFemalebusinessActa Paediatrica
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Pregnancy in advanced maternal age: maternal and fetal outcome.

2014

The objective of this research is to evaluate maternal and fetal outcome of pregnant women over 40 years. The outcome has been evaluated through the following data: age, nationality, number of deliveries, complications of pregnancy, type of delivery, newborn's weight and APGAR index. 201 pregnant women have been recruited. The GDM has been observed in 11 women (5.5%). The antepartum haemorrhage has been observed in 7 women (3.5%). The cesarean section rate was 76% in the Group of primiparae woman and 64% in the Group of multiparae. The incidence of Children LBW (low Birth weight) was 17% in the primiparae and 10% in the multiparare.

medicine.medical_specialtyPregnancyadvanced maternal age maternal outcome fetal outcomeObstetricsbusiness.industrymedicineFetal outcomeAdvanced maternal agemedicine.diseasebusinessSettore MED/40 - Ginecologia E Ostetricia
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