Fetus prenatal diagnosis. Medical search. Frequent questions

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Anatomy22

Fetus Amniotic Fluid Fetal Heart Chorionic Villi Chromosomes, Human, Pair 18 Fetal Blood Chromosomes, Human, Pair 13 Placenta Umbilical Cord Umbilical Arteries X Chromosome Chromosomes, Human, Pair 21 Neck Cloaca Chromosomes, Human, Pair 22 Azygos Vein Sacrococcygeal Region Chromosomes, Human, X Vena Cava, Inferior Foramen Ovale Meconium Thorax

Organisms3

Campylobacter fetus Tritrichomonas foetus Sheep

Diseases116

Fetal Diseases Prenatal Exposure Delayed Effects Abnormalities, Multiple Chromosome Disorders Trisomy Hydrops Fetalis Fetal Death Down Syndrome Thalassemia Heart Defects, Congenital Congenital Abnormalities Polyhydramnios Sex Chromosome Disorders Hemoglobinopathies Ectromelia Syndrome Twins, Conjoined Hernia, Umbilical beta-Thalassemia Aneuploidy Sex Chromosome Aberrations Chromosome Aberrations Genetic Diseases, Inborn Gastroschisis Prenatal Injuries Hernia, Diaphragmatic Dandy-Walker Syndrome Hydrocolpos Oligohydramnios Musculoskeletal Abnormalities Pulmonary Atresia Levocardia Pregnancy Complications Anencephaly Fetomaternal Transfusion Fetal Growth Retardation Anus, Imperforate Adrenal Hyperplasia, Congenital Agenesis of Corpus Callosum Neural Tube Defects Muscular Dystrophies Spinal Muscular Atrophies of Childhood Hypoplastic Left Heart Syndrome Micrognathism Spinal Dysraphism Cystic Adenomatoid Malformation of Lung, Congenital Hydronephrosis Amniotic Band Syndrome Meningomyelocele Toxoplasmosis, Congenital Encephalocele Intestinal Atresia Bone Diseases, Developmental alpha-Thalassemia Heart Septal Defects Holoprosencephaly Lymphangioma, Cystic Respiratory System Abnormalities Citrullinemia Urogenital Abnormalities Metabolism, Inborn Errors Amino Acid Metabolism, Inborn Errors Hydrocephalus Meningocele Ornithine Carbamoyltransferase Deficiency Disease Spina Bifida Occulta Lymphangioma Hemophilia A Cystic Fibrosis Rare Diseases Hypophosphatasia Arthrogryposis XYY Karyotype Clubfoot Bronchopulmonary Sequestration Microcephaly Epidermolysis Bullosa Abortion, Spontaneous Fetal Alcohol Spectrum Disorders Tricuspid Atresia Cri-du-Chat Syndrome Foot Deformities, Congenital Lipidoses Abortion, Veterinary Klippel-Trenaunay-Weber Syndrome Turner Syndrome Prune Belly Syndrome Cleft Lip Chondrodysplasia Punctata Placenta Diseases Aortic Arch Syndromes Anemia, Sickle Cell Cleft Palate Polydactyly 46, XY Disorders of Sex Development Aortopulmonary Septal Defect Bladder Exstrophy Chromosome Deletion Ichthyosis, Lamellar Klinefelter Syndrome Thoracic Diseases Intellectual Disability Diseases in Twins Hemophilia B Limb Deformities, Congenital Skin Abnormalities Cysts Fetal Weight Fetal Hypoxia Arteriovenous Malformations Pregnancy Complications, Infectious Urethral Obstruction Luteoma Ureterocele Dilatation, Pathologic Polycystic Kidney Diseases

Chemicals and Drugs8

Genetic Markers DNA Steroid 21-Hydroxylase Globins DNA Probes alpha-Fetoproteins alpha-Globins Biological Markers

Analytical, Diagnostic and Therapeutic Techniques and Equipment63

Prenatal Diagnosis Ultrasonography, Prenatal Chorionic Villi Sampling Amniocentesis Prenatal Care Abortion, Eugenic Heterozygote Detection Abortion, Therapeutic Abortion, Induced Cordocentesis Pregnancy Outcome Karyotyping Genetic Testing Sensitivity and Specificity Pedigree Ultrasonography, Doppler, Color Retrospective Studies Preimplantation Diagnosis Sex Determination Analysis Polymerase Chain Reaction Fetoscopy Delayed Diagnosis Fatal Outcome Early Diagnosis Echocardiography, Four-Dimensional Prospective Studies Magnetic Resonance Imaging Ultrasonography, Doppler, Pulsed Nuchal Translucency Measurement Imaging, Three-Dimensional Abortion, Legal Reproducibility of Results DNA Mutational Analysis Diagnosis Ultrasonography Diagnostic Errors Risk Factors Predictive Value of Tests In Situ Hybridization, Fluorescence Echoencephalography Follow-Up Studies Ultrasonography, Doppler Cesarean Section Biopsy Cohort Studies Autopsy Neonatal Screening Prognosis Prevalence Crown-Rump Length Clinical Enzyme Tests Postnatal Care False Positive Reactions Echocardiography Incidence Tomography, X-Ray Computed Questionnaires Treatment Outcome Fetal Weight Echocardiography, Doppler, Color False Negative Reactions Perinatal Care Diagnosis, Computer-Assisted

Psychiatry and Psychology4

Maternal-Fetal Relations Mothers 46, XY Disorders of Sex Development Intellectual Disability

Phenomena and Processes45

Pregnancy Gestational Age Pregnancy Trimester, Second Trisomy Pregnancy Trimester, First Pregnancy Outcome Pregnancy Trimester, Third Sensitivity and Specificity Maternal-Fetal Exchange Aneuploidy Sex Chromosome Aberrations Chromosome Aberrations Chromosomes, Human, Pair 18 Maternal Age Chromosomes, Human, Pair 13 Mosaicism Genetic Linkage Pregnancy, High-Risk Genetic Markers Fetal Development Polymorphism, Restriction Fragment Length Heterozygote Mutation Karyotype X Chromosome Chromosomes, Human, Pair 21 Genes, Recessive Consanguinity Time Factors Embryonic and Fetal Development Chromosomes, Human, Pair 22 Pregnancy Trimesters Crown-Rump Length XYY Karyotype Heart Rate, Fetal Base Sequence Chromosomes, Human, X Alleles Homozygote Chromosome Deletion Phenotype Genotype Polymorphism, Genetic Fetal Weight Pregnancy, Multiple

Disciplines and Occupations2

Genetic Counseling Perinatology

Anthropology, Education, Sociology and Social Phenomena2

Mothers Autopsy

Humanities2

Postmodernism Ethics, Medical

Information Science7

Fatal Outcome Imaging, Three-Dimensional Prevalence Base Sequence Incidence Questionnaires Diagnosis, Computer-Assisted

Named Groups4

Infant, Newborn Pregnant Women Mothers Triplets

Health Care25

Prenatal Care Genetic Counseling Genetic Testing Sensitivity and Specificity Retrospective Studies Fatal Outcome Maternal Age Maternal Exposure Genetic Services Prospective Studies Reproducibility of Results Diagnostic Errors Risk Factors Predictive Value of Tests Follow-Up Studies Cohort Studies Neonatal Screening Prevalence Crown-Rump Length Postnatal Care Incidence Questionnaires Treatment Outcome Ethics, Medical Perinatal Care

Geographicals1

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Humanities Information Science Named Groups Health Care Geographicals

Prenatal Diagnosis Fetus Fetal Diseases Pregnancy Ultrasonography, Prenatal Chorionic Villi Sampling Prenatal Exposure Delayed Effects Amniocentesis Prenatal Care Abortion, Eugenic Gestational Age Heterozygote Detection Amniotic Fluid Infant, Newborn Genetic Counseling Abortion, Therapeutic Pregnancy Trimester, Second Abnormalities, Multiple Abortion, Induced Chromosome Disorders Trisomy Pregnancy Trimester, First Hydrops Fetalis Fetal Death Cordocentesis Down Syndrome Pregnancy Outcome Thalassemia Fetal Heart Karyotyping Campylobacter fetus Genetic Testing Pregnancy Trimester, Third Heart Defects, Congenital Congenital Abnormalities Polyhydramnios Sensitivity and Specificity Tritrichomonas foetus Sex Chromosome Disorders Hemoglobinopathies Pedigree Maternal-Fetal Exchange Ultrasonography, Doppler, Color Retrospective Studies Preimplantation Diagnosis Ectromelia Sex Determination Analysis Chorionic Villi Polymerase Chain Reaction Syndrome Twins, Conjoined Hernia, Umbilical Fetoscopy beta-Thalassemia Aneuploidy Sex Chromosome Aberrations Chromosome Aberrations Pregnant Women Chromosomes, Human, Pair 18 Genetic Diseases, Inborn Gastroschisis Delayed Diagnosis Fatal Outcome Prenatal Injuries Hernia, Diaphragmatic Dandy-Walker Syndrome Hydrocolpos Fetal Blood Maternal Age Oligohydramnios Musculoskeletal Abnormalities Chromosomes, Human, Pair 13 Early Diagnosis Pulmonary Atresia Mosaicism Echocardiography, Four-Dimensional Placenta Levocardia Genetic Linkage Pregnancy, High-Risk Pregnancy Complications Anencephaly Fetomaternal Transfusion Fetal Growth Retardation Anus, Imperforate Adrenal Hyperplasia, Congenital Maternal Exposure Genetic Services Agenesis of Corpus Callosum Genetic Markers Fetal Development Prospective Studies DNA Neural Tube Defects Muscular Dystrophies Spinal Muscular Atrophies of Childhood Magnetic Resonance Imaging Ultrasonography, Doppler, Pulsed Hypoplastic Left Heart Syndrome Micrognathism

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