Syndrome prenatal diagnosis. Medical search. Frequent questions

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Anatomy18

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

Diseases130

Syndrome Fetal Diseases Prenatal Exposure Delayed Effects Down Syndrome Abnormalities, Multiple Chromosome Disorders Trisomy Thalassemia Hydrops Fetalis Metabolic Syndrome X Fetal Death Heart Defects, Congenital Sex Chromosome Disorders Congenital Abnormalities Polyhydramnios Hemoglobinopathies Ectromelia Sex Chromosome Aberrations Hernia, Umbilical Turner Syndrome Genetic Diseases, Inborn Chromosome Aberrations beta-Thalassemia Aneuploidy Twins, Conjoined Nephrotic Syndrome Sjogren's Syndrome Musculoskeletal Abnormalities Dandy-Walker Syndrome Prenatal Injuries Hydrocolpos Anus, Imperforate Klinefelter Syndrome Gastroschisis Pulmonary Atresia Levocardia Adrenal Hyperplasia, Congenital Hypoplastic Left Heart Syndrome DiGeorge Syndrome Fetomaternal Transfusion Agenesis of Corpus Callosum Micrognathism Hernia, Diaphragmatic Muscular Dystrophies Prader-Willi Syndrome Oligohydramnios Spinal Muscular Atrophies of Childhood Encephalocele Anencephaly Intellectual Disability Pregnancy Complications Neural Tube Defects Myelodysplastic Syndromes Bone Diseases, Developmental Cushing Syndrome Spinal Dysraphism Hydronephrosis Cystic Adenomatoid Malformation of Lung, Congenital Polycystic Ovary Syndrome Amniotic Band Syndrome Toxoplasmosis, Congenital Meningomyelocele Acute Coronary Syndrome Microcephaly Cri-du-Chat Syndrome Intestinal Atresia Urogenital Abnormalities Rare Diseases Heart Septal Defects Williams Syndrome Foot Deformities, Congenital Metabolism, Inborn Errors Chromosome Deletion alpha-Thalassemia Meningocele Goldenhar Syndrome Horner Syndrome Arthrogryposis Citrullinemia Lymphangioma, Cystic Holoprosencephaly Respiratory System Abnormalities Prune Belly Syndrome Amino Acid Metabolism, Inborn Errors Ectodermal Dysplasia Long QT Syndrome Hemophilia A Hydrocephalus Skin Abnormalities Ornithine Carbamoyltransferase Deficiency Disease Spina Bifida Occulta Cystic Fibrosis Hand Deformities, Congenital XYY Karyotype Lymphangioma Guillain-Barre Syndrome Limb Deformities, Congenital Polydactyly Fetal Alcohol Spectrum Disorders Hemolytic-Uremic Syndrome Hypophosphatasia Epidermolysis Bullosa Clubfoot Cleft Lip Tricuspid Atresia Chondrodysplasia Punctata Aortic Arch Syndromes Antiphospholipid Syndrome Tourette Syndrome Cleft Palate Compartment Syndromes Anemia, Sickle Cell Klippel-Trenaunay-Weber Syndrome Bronchopulmonary Sequestration Lipidoses Carpal Tunnel Syndrome Scimitar Syndrome Ichthyosis, Lamellar 46, XY Disorders of Sex Development Thoracic Diseases Porcine Reproductive and Respiratory Syndrome Immunologic Deficiency Syndromes Diseases in Twins Short Rib-Polydactyly Syndrome Aortopulmonary Septal Defect Dwarfism Reye Syndrome Bladder Exstrophy Bartter Syndrome HELLP Syndrome

Chemicals and Drugs7

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment58

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

Psychiatry and Psychology5

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

Phenomena and Processes40

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

Disciplines and Occupations2

Genetic Counseling Perinatology

Anthropology, Education, Sociology and Social Phenomena2

Mothers Autopsy

Humanities1

Information Science7

Fatal Outcome Prevalence Imaging, Three-Dimensional Base Sequence Incidence Molecular Sequence Data Questionnaires

Named Groups3

Infant, Newborn Pregnant Women Mothers

Health Care25

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

Geographicals2

Israel United States

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 Information Science Named Groups Health Care

Prenatal Diagnosis Syndrome Fetal Diseases Pregnancy Ultrasonography, Prenatal Chorionic Villi Sampling Prenatal Exposure Delayed Effects Amniocentesis Prenatal Care Abortion, Eugenic Heterozygote Detection Down Syndrome Genetic Counseling Abnormalities, Multiple Infant, Newborn Abortion, Therapeutic Amniotic Fluid Gestational Age Pregnancy Trimester, Second Abortion, Induced Fetus Chromosome Disorders Pregnancy Outcome Trisomy Genetic Testing Thalassemia Karyotyping Pedigree Cordocentesis Pregnancy Trimester, First Hydrops Fetalis Metabolic Syndrome X Fetal Death Sensitivity and Specificity Heart Defects, Congenital Sex Chromosome Disorders Congenital Abnormalities Polyhydramnios Retrospective Studies Hemoglobinopathies Pregnancy Trimester, Third Ectromelia Polymerase Chain Reaction Preimplantation Diagnosis Sex Chromosome Aberrations Fatal Outcome Hernia, Umbilical Ultrasonography, Doppler, Color Turner Syndrome Genetic Diseases, Inborn Chromosome Aberrations Pregnant Women beta-Thalassemia Sex Determination Analysis Fetal Heart Chorionic Villi Aneuploidy Twins, Conjoined Nephrotic Syndrome Fetoscopy Delayed Diagnosis Chromosomes, Human, Pair 18 Sjogren's Syndrome Mutation Mosaicism Musculoskeletal Abnormalities Genetic Linkage Dandy-Walker Syndrome Prenatal Injuries Early Diagnosis Hydrocolpos DNA Mutational Analysis Magnetic Resonance Imaging Risk Factors Maternal Age Prospective Studies Anus, Imperforate Genetic Markers Klinefelter Syndrome Chromosomes, Human, Pair 13 Gastroschisis Pulmonary Atresia Levocardia Adrenal Hyperplasia, Congenital Hypoplastic Left Heart Syndrome DNA DiGeorge Syndrome Heterozygote Genetic Services Fetomaternal Transfusion Agenesis of Corpus Callosum Micrognathism Hernia, Diaphragmatic Echocardiography, Four-Dimensional Muscular Dystrophies Prader-Willi Syndrome Oligohydramnios Pregnancy, High-Risk Genes, Recessive Consanguinity

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