Prenatal diagnosis fetal cordocentesis. Medical search. Frequent questions

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Anatomy16

Fetal Blood Amniotic Fluid Fetus Fetal Heart Chorionic Villi Chromosomes, Human, Pair 18 Chromosomes, Human, Pair 13 X Chromosome Chromosomes, Human, Pair 21 Cloaca Umbilical Cord Azygos Vein Chromosomes, Human, Pair 22 Sacrococcygeal Region Chromosomes, Human, X Neck

Diseases94

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

Chemicals and Drugs5

Genetic Markers DNA Steroid 21-Hydroxylase Globins DNA Probes

Analytical, Diagnostic and Therapeutic Techniques and Equipment53

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

Psychiatry and Psychology3

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

Phenomena and Processes36

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

Disciplines and Occupations2

Genetic Counseling Perinatology

Anthropology, Education, Sociology and Social Phenomena2

Mothers Autopsy

Humanities1

Information Science5

Fatal Outcome Imaging, Three-Dimensional Prevalence Base Sequence Questionnaires

Named Groups3

Infant, Newborn Pregnant Women Mothers

Health Care20

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

Geographicals1

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

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