Neurodevelopmental syndromes. Medical search. Frequent questions

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Anatomy16

Brain Nervous System Cerebral Ventricles Chromosomes, Human, Pair 15 Neurons Chromosomes, Human, Pair 22 Cerebral Cortex Central Nervous System Septum Pellucidum Corpus Callosum Chromosomes, Human, X Neural Pathways Hippocampus Head Cerebellum Chromosomes, Human, Pair 7

Organisms4

Animals, Newborn Porcine respiratory and reproductive syndrome virus Mice, Knockout Mice, Inbred C57BL

Diseases127

Syndrome Rett Syndrome Nervous System Diseases Psychomotor Disorders Down Syndrome Cerebral Palsy Metabolic Syndrome X Williams Syndrome Infant, Premature, Diseases Leukomalacia, Periventricular Intellectual Disability Angelman Syndrome Prenatal Exposure Delayed Effects Abnormalities, Multiple Nephrotic Syndrome Prader-Willi Syndrome Sjogren's Syndrome Asphyxia Neonatorum Learning Disorders Turner Syndrome Agenesis of Corpus Callosum Brain Diseases Hypoxia-Ischemia, Brain Tourette Syndrome Brain Damage, Chronic Respiratory Distress Syndrome, Newborn Disease Models, Animal Myelodysplastic Syndromes Central Nervous System Diseases Nervous System Malformations Cushing Syndrome Bronchopulmonary Dysplasia Microcephaly Acute Coronary Syndrome Polycystic Ovary Syndrome Mercury Poisoning, Nervous System Seizures Hypoplastic Left Heart Syndrome DiGeorge Syndrome Horner Syndrome Long QT Syndrome Fetal Alcohol Spectrum Disorders Heredodegenerative Disorders, Nervous System Guillain-Barre Syndrome Macrocephaly Hemolytic-Uremic Syndrome Infant, Newborn, Diseases Genetic Predisposition to Disease Facies Hydrocephalus Compartment Syndromes Heart Defects, Congenital Antiphospholipid Syndrome Spasms, Infantile Porcine Reproductive and Respiratory Syndrome Craniofacial Abnormalities Klinefelter Syndrome Carpal Tunnel Syndrome Dandy-Walker Syndrome Language Development Disorders Werner Syndrome Neurotoxicity Syndromes Intracranial Hemorrhages Reye Syndrome Blindness Epilepsy Craniosynostoses Bartter Syndrome Hearing Loss, Bilateral Communication Disorders Fetofetal Transfusion HELLP Syndrome Chromosome Deletion Encephalomalacia Bloom Syndrome Brugada Syndrome Ehlers-Danlos Syndrome Fragile X Syndrome Eye Abnormalities Respiratory Distress Syndrome, Adult Severe Acute Respiratory Syndrome Restless Legs Syndrome Chromosome Duplication Job Syndrome Wiskott-Aldrich Syndrome Premature Birth Paraneoplastic Syndromes Enterocolitis, Necrotizing Sweet Syndrome Neuronal Migration Disorders Cerebral Hemorrhage Intestinal Perforation Acquired Immunodeficiency Syndrome Malformations of Cortical Development Birth Weight Churg-Strauss Syndrome Growth Disorders Sturge-Weber Syndrome Erythroblastosis, Fetal Ataxia Budd-Chiari Syndrome Neuromuscular Diseases Epilepsy, Rolandic Chediak-Higashi Syndrome Polyhydramnios Diseases in Twins Chromosome Disorders Wolff-Parkinson-White Syndrome Hyperbilirubinemia, Neonatal Kallmann Syndrome Hearing Loss Sick Sinus Syndrome Deafness Stevens-Johnson Syndrome Pregnancy Complications Sezary Syndrome Felty Syndrome Usher Syndromes Beckwith-Wiedemann Syndrome Facial Asymmetry Deaf-Blind Disorders Movement Disorders Alagille Syndrome Congenital Abnormalities Bardet-Biedl Syndrome ACTH Syndrome, Ectopic Peutz-Jeghers Syndrome

Chemicals and Drugs11

Methyl-CpG-Binding Protein 2 Methylmercury Compounds Nerve Tissue Proteins Environmental Pollutants Chlorpyrifos Anticonvulsants Biological Markers Hemosiderin Thimerosal Halogenated Diphenyl Ethers Cell Adhesion Molecules, Neuronal

Analytical, Diagnostic and Therapeutic Techniques and Equipment36

Neurologic Examination Magnetic Resonance Imaging Follow-Up Studies Echoencephalography Risk Factors Disease Models, Animal Prospective Studies Norwood Procedures Treatment Outcome Cohort Studies Pedigree Case-Control Studies Facies Retrospective Studies Severity of Illness Index Neuroimaging Intensive Care, Neonatal Hypothermia, Induced Prenatal Diagnosis Electroencephalography Diagnostic Techniques, Neurological Longitudinal Studies Prognosis DNA Mutational Analysis Risk Assessment Birth Weight Analysis of Variance Prevalence Incidence Blood Transfusion, Intrauterine Dermatoglyphics Reference Values Genetic Association Studies Predictive Value of Tests Cardiac Surgical Procedures Startle Reaction

Psychiatry and Psychology34

Developmental Disabilities Child Development Autistic Disorder Psychomotor Disorders Intellectual Disability Child Development Disorders, Pervasive Schizophrenia Learning Disorders Motor Skills Disorders Intelligence Neuropsychological Tests Tourette Syndrome Cognition Disorders Intelligence Tests Cognition Motor Skills Behavior, Animal Psychomotor Performance Mental Disorders Attention Deficit Disorder with Hyperactivity Communication Disorders Schizophrenic Psychology Child Behavior Disorders Social Behavior Restless Legs Syndrome Stereotyped Behavior Motor Activity Adolescent Development Critical Period (Psychology)Psychotic Disorders Language Development Infant Behavior Wechsler Scales Startle Reaction

Phenomena and Processes29

Child Development Pregnancy Gestational Age Phenotype Mutation Chromosomes, Human, Pair 15 Genetic Predisposition to Disease Time Factors Chromosomes, Human, Pair 22 Psychomotor Performance Neurogenesis DNA Copy Number Variations Chromosome Deletion Chromosome Duplication Genotype Birth Weight Motor Activity Chromosomes, Human, X Adolescent Development Haploinsufficiency Genomic Imprinting Heterozygote Mutation, Missense Sensory Gating Gene Expression Regulation, Developmental Chromosomes, Human, Pair 7 Startle Reaction Endophenotypes Paternal Age

Anthropology, Education, Sociology and Social Phenomena3

Social Behavior Disorders Adoption Dermatoglyphics

Information Science3

Prevalence Incidence Molecular Sequence Data

Named Groups7

Infant, Newborn Infant, Extremely Low Birth Weight Infant, Premature Infant, Extremely Premature Infant, Very Low Birth Weight Child, Institutionalized Twins

Health Care21

Follow-Up Studies Risk Factors Prospective Studies Treatment Outcome Cohort Studies Case-Control Studies Retrospective Studies Severity of Illness Index Age Factors Intensive Care, Neonatal Maternal Exposure Intensive Care Units, Neonatal Longitudinal Studies Risk Assessment Analysis of Variance Prevalence Incidence Age of Onset Predictive Value of Tests Family Health Sex Factors

Geographicals1

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

Syndrome Developmental Disabilities Child Development Rett Syndrome Infant, Newborn Methyl-CpG-Binding Protein 2 Nervous System Diseases Autistic Disorder Psychomotor Disorders Down Syndrome Infant, Extremely Low Birth Weight Infant, Premature Cerebral Palsy Metabolic Syndrome X Williams Syndrome Infant, Premature, Diseases Brain Leukomalacia, Periventricular Intellectual Disability Child Development Disorders, Pervasive Schizophrenia Angelman Syndrome Pregnancy Nervous System Prenatal Exposure Delayed Effects Neurologic Examination Abnormalities, Multiple Nephrotic Syndrome Prader-Willi Syndrome Sjogren's Syndrome Infant, Extremely Premature Asphyxia Neonatorum Magnetic Resonance Imaging Learning Disorders Gestational Age Follow-Up Studies Echoencephalography Turner Syndrome Motor Skills Disorders Infant, Very Low Birth Weight Agenesis of Corpus Callosum Intelligence Neuropsychological Tests Phenotype Brain Diseases Hypoxia-Ischemia, Brain Tourette Syndrome Brain Damage, Chronic Cognition Disorders Risk Factors Intelligence Tests Respiratory Distress Syndrome, Newborn Disease Models, Animal Myelodysplastic Syndromes Central Nervous System Diseases Nervous System Malformations Cushing Syndrome Bronchopulmonary Dysplasia Mutation Microcephaly Acute Coronary Syndrome Polycystic Ovary Syndrome Prospective Studies Mercury Poisoning, Nervous System Seizures Hypoplastic Left Heart Syndrome Norwood Procedures DiGeorge Syndrome Treatment Outcome Cerebral Ventricles Horner Syndrome Cohort Studies Cognition Long QT Syndrome Fetal Alcohol Spectrum Disorders Pedigree Heredodegenerative Disorders, Nervous System Case-Control Studies Chromosomes, Human, Pair 15 Guillain-Barre Syndrome Motor Skills Macrocephaly Hemolytic-Uremic Syndrome Methylmercury Compounds Infant, Newborn, Diseases Genetic Predisposition to Disease Animals, Newborn Time Factors Seychelles Facies Hydrocephalus Compartment Syndromes Heart Defects, Congenital Neurons Antiphospholipid Syndrome Chromosomes, Human, Pair 22 Retrospective Studies Spasms, Infantile Behavior, Animal Porcine Reproductive and Respiratory Syndrome

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