Abnormalities in fetal prenatal diagnosis. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy21

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

Diseases114

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

Chemicals and Drugs9

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment67

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

Psychiatry and Psychology4

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

Phenomena and Processes44

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

Disciplines and Occupations2

Genetic Counseling Perinatology

Anthropology, Education, Sociology and Social Phenomena2

Mothers Autopsy

Humanities2

Postmodernism Ethics, Medical

Information Science8

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

Named Groups4

Infant, Newborn Pregnant Women Mothers Triplets

Health Care29

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

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 Humanities Information Science Named Groups Health Care Geographicals

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

No FAQ available that match "abnormalities in fetal prenatal diagnosis"