Chromosomal abnormality congenital abnormalities. Medical search. Frequent questions

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Anatomy55

Chromosomes, Human, 6-12 and X Chromosomes, Human, Pair 13 Chromosomes, Human, Pair 18 Fetus Chromosomes, Human, Y Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 11 Chromosomes, Human, X Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 1 Chromosomes, Human Chromosomes, Human, Pair 12 Neck Chromosomes, Human, Pair 17 Chromosomes, Human, 4-5 Fetal Heart Spermatozoa Chromosome Structures Chromosomes, Human, 1-3 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 3 Chromosomes, Human, 21-22 and Y Chromosomes, Human, 16-18 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 5 Chromosomes, Human, 13-15 Sex Chromosomes Bone Marrow Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 9 Blastocyst Ring Chromosomes Cleavage Stage, Ovum Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 4 Philadelphia Chromosome Y Chromosome Brain Chromosomes Embryo, Mammalian Blastomeres X Chromosome Bone Marrow Cells Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 19 Clone Cells Cells, Cultured Umbilical Arteries Amniotic Fluid Telomere Oocytes

Diseases86

Congenital Abnormalities Chromosome Aberrations Chromosome Disorders Abnormalities, Multiple Abnormalities, Drug-Induced Arthrogryposis Hydranencephaly Trisomy Aneuploidy Translocation, Genetic Fetal Diseases Sex Chromosome Aberrations Abortion, Spontaneous Arbovirus Infections Fanconi Anemia Intellectual Disability Urogenital Abnormalities Heart Defects, Congenital Limb Deformities, Congenital Abnormal Karyotype Pregnancy Complications Crisscross Heart Syndrome Cryptorchidism Fetal Death Azoospermia Sex Chromosome Disorders of Sex Development Down Syndrome Chromosome Deletion Hypospadias Infertility, Male Monosomy Oligospermia Triploidy Anemia, Refractory XYY Karyotype Myelodysplastic Syndromes Turner Syndrome Klinefelter Syndrome Abortion, Habitual Uniparental Disomy Chromosome Inversion Hernia, Umbilical Leukemia, Myeloid, Acute Leukemia, Myeloid Chromosomal Instability Birth Weight Abnormalities, Severe Teratoid Eye Abnormalities Abortion, Missed Leukemia, Plasma Cell Leukemia Leukemia, Lymphocytic, Chronic, B-Cell Ring Chromosomes Primary Ovarian Insufficiency Amenorrhea Precursor Cell Lymphoblastic Leukemia-Lymphoma Acute Disease Chromosome Duplication Multiple Myeloma Holoprosencephaly Anemia, Refractory, with Excess of Blasts Chromosome Breakage Philadelphia Chromosome Cardiovascular Abnormalities Craniofacial Abnormalities Anencephaly Genomic Instability Skin Abnormalities Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative Leukemia-Lymphoma, Adult T-Cell Leukemia, Lymphoid Leukemia, Myelogenous, Chronic, BCR-ABL Positive Musculoskeletal Abnormalities Hernia, Diaphragmatic Blast Crisis Tooth Abnormalities Leukemia, Myelomonocytic, Acute Myeloproliferative Disorders Leukemia, Myeloid, Chronic-Phase Disease Progression Infertility, Female Cell Transformation, Neoplastic Lymphoma Polyploidy Disease Models, Animal

Chemicals and Drugs17

Fanconi Anemia Complementation Group Proteins Teratogens 6-Mercaptopurine Sulfasalazine Azathioprine Oncogene Proteins, Fusion Myeloid-Lymphoid Leukemia Protein Chorionic Gonadotropin, beta Subunit, Human Pregnancy-Associated Plasma Protein-A DNA, Neoplasm Core Binding Factor Alpha 2 Subunit Gonadotropins DNA-Binding Proteins DNA Probes Genetic Markers Transcription Factors Neoplasm Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment56

Karyotyping In Situ Hybridization, Fluorescence Ultrasonography, Prenatal Cytogenetic Analysis Prenatal Diagnosis Pregnancy Outcome Dermatoglyphics Chromosome Banding Perinatal Care Amniocentesis Retrospective Studies Preconception Care Spectral Karyotyping Preimplantation Diagnosis Pedigree Incidence Risk Factors Case-Control Studies Magnetic Resonance Imaging Nuchal Translucency Measurement Infant Mortality Cohort Studies Prospective Studies Abortion, Eugenic Tomography, X-Ray Computed Chorionic Villi Sampling Sperm Injections, Intracytoplasmic Crown-Rump Length Prognosis Birth Weight Treatment Outcome Sensitivity and Specificity Fertilization in Vitro Comparative Genomic Hybridization Reproductive Techniques, Assisted Genetic Testing Chromosome Mapping Multiplex Polymerase Chain Reaction Nucleic Acid Hybridization Polymerase Chain Reaction Semen Analysis Predictive Value of Tests Follow-Up Studies Prevalence Biopsy Reference Values Oligonucleotide Array Sequence Analysis Chromosome Painting Sperm Count Immunophenotyping DNA Mutational Analysis Gene Expression Profiling Electrocardiography Fatal Outcome Reverse Transcriptase Polymerase Chain Reaction Disease Models, Animal

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes91

Chromosome Aberrations Pregnancy Trisomy Aneuploidy Translocation, Genetic Sex Chromosome Aberrations Pregnancy Trimester, First Pregnancy Outcome Chromosomes, Human, 6-12 and X Abnormal Karyotype Gestational Age Chromosomes, Human, Pair 13 Maternal Age Mosaicism Chromosomes, Human, Pair 18 Chromosome Deletion Karyotype Stillbirth Phenotype Chromosomes, Human, Y Chromosomes, Human, Pair 8 Monosomy Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 11 Triploidy Chromosomes, Human, X XYY Karyotype Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 1 Chromosomes, Human Pregnancy Trimester, Second Chromosomes, Human, Pair 12 Pregnancy, High-Risk Chromosomes, Human, Pair 17 Chromosomes, Human, 4-5 Chromosome Structures Ploidies Diploidy Chromosomes, Human, 1-3 Uniparental Disomy Chromosome Inversion Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 3 Metaphase Chromosomes, Human, 21-22 and Y Chromosomes, Human, 16-18 Crown-Rump Length Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 5 Chromosomal Instability Chromosomes, Human, 13-15 Sex Chromosomes Birth Weight Gene Rearrangement Chromosomes, Human, Pair 6 Sensitivity and Specificity Mutation Chromosomes, Human, Pair 20 Gene Dosage Chromosomes, Human, Pair 9 Ring Chromosomes Interphase Chromosome Duplication Chromosomes, Human, Pair 2 Chromosome Breakage Nucleic Acid Hybridization Chromosomes, Human, Pair 4 Philadelphia Chromosome Gene Deletion Y Chromosome Time Factors Chromosomes Genomic Instability Base Sequence Embryonic and Fetal Development Oncogene Fusion X Chromosome Embryonic Development Chromosomes, Human, Pair 10 Heterozygote Chromosomes, Human, Pair 19 Loss of Heterozygosity Sperm Count Genetic Markers Spermatogenesis Proto-Oncogenes Meiosis Telomere Polyploidy

Disciplines and Occupations2

Cytogenetics Genetic Counseling

Anthropology, Education, Sociology and Social Phenomena1

Dermatoglyphics

Information Science6

Incidence Infant Mortality Base Sequence Prevalence Molecular Sequence Data Fatal Outcome

Named Groups2

Infant, Newborn Infant, Premature

Health Care21

Maternal Age Paternal Exposure Perinatal Care Retrospective Studies Preconception Care Incidence Risk Factors Case-Control Studies Infant Mortality Cohort Studies Prospective Studies Crown-Rump Length Treatment Outcome Sensitivity and Specificity Genetic Testing Genetic Counseling Predictive Value of Tests Follow-Up Studies Prevalence Age Factors Fatal Outcome

Geographicals6

Hungary Denmark England Turkey Ukraine Iran

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 Geographicals

Congenital Abnormalities Chromosome Aberrations Chromosome Disorders Abnormalities, Multiple Karyotyping Hungary Pregnancy Abnormalities, Drug-Induced Infant, Newborn Arthrogryposis Hydranencephaly Trisomy Aneuploidy Translocation, Genetic In Situ Hybridization, Fluorescence Fetal Diseases Sex Chromosome Aberrations Ultrasonography, Prenatal Abortion, Spontaneous Cytogenetic Analysis Prenatal Diagnosis Arbovirus Infections Fanconi Anemia Pregnancy Trimester, First Intellectual Disability Urogenital Abnormalities Heart Defects, Congenital Pregnancy Outcome Chromosomes, Human, 6-12 and X Limb Deformities, Congenital Abnormal Karyotype Gestational Age Pregnancy Complications Crisscross Heart Syndrome Fanconi Anemia Complementation Group Proteins Chromosomes, Human, Pair 13 Cryptorchidism Fetal Death Azoospermia Dermatoglyphics Cytogenetics Maternal Age Mosaicism Chromosome Banding Sex Chromosome Disorders of Sex Development Paternal Exposure Down Syndrome Chromosomes, Human, Pair 18 Chromosome Deletion Karyotype Stillbirth Fetus Perinatal Care Hypospadias Teratogens Amniocentesis Retrospective Studies Infertility, Male 6-Mercaptopurine Preconception Care Phenotype Chromosomes, Human, Y Chromosomes, Human, Pair 8 Monosomy Oligospermia Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 11 Spectral Karyotyping Triploidy Chromosomes, Human, X Preimplantation Diagnosis Anemia, Refractory Pedigree XYY Karyotype Sulfasalazine Incidence Chromosomes, Human, Pair 21 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 1 Chromosomes, Human Myelodysplastic Syndromes Pregnancy Trimester, Second Chromosomes, Human, Pair 12 Risk Factors Azathioprine Neck Pregnancy, High-Risk Chromosomes, Human, Pair 17 Case-Control Studies Magnetic Resonance Imaging Nuchal Translucency Measurement Infant Mortality Cohort Studies Prospective Studies Denmark Chromosomes, Human, 4-5 Turner Syndrome Klinefelter Syndrome Fetal Heart

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