Causes of developmental delays. Medical search. Frequent questions

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Anatomy25

Face Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 16 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 13 Brain Chromosomes, Human, X Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 4 Chromosomes, Human, Pair 17 Facial Bones Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 12 Tooth, Deciduous Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 7 Chromosomes, Human, Pair 5 Cerebellum Fibroblasts Cerebral Cortex Cells, Cultured

Organisms4

Larva Mice, Knockout Mice, Inbred C57BL Drosophila melanogaster

Diseases71

Intellectual Disability Abnormalities, Multiple Microcephaly Muscle Hypotonia Syndrome Chromosome Duplication Chromosome Deletion Facies Failure to Thrive Craniofacial Abnormalities Language Development Disorders Growth Disorders Communication Disorders Chromosome Disorders Brain Diseases, Metabolic, Inborn Spasms, Infantile Agenesis of Corpus Callosum Osteopoikilosis Epilepsy Psychomotor Disorders Tetrasomy Metabolism, Inborn Errors Nervous System Malformations Hand Deformities, Congenital Trisomy Seizures Cerebral Palsy Asphyxia Neonatorum Angelman Syndrome Blepharophimosis Craniosynostoses Eye Abnormalities Learning Disorders Dwarfism Chromosome Breakage Prader-Willi Syndrome Kernicterus Chromosome Aberrations Sex Chromosome Aberrations Malformations of Cortical Development Prenatal Exposure Delayed Effects Embryo Loss Infant, Premature, Diseases Purine-Pyrimidine Metabolism, Inborn Errors Foot Deformities, Congenital Congenital Hypothyroidism Neurocutaneous Syndromes De Lange Syndrome Abnormalities, Drug-Induced Coloboma Down Syndrome Sinus Pericranii Translocation, Genetic Cutis Laxa Fetal Alcohol Spectrum Disorders Ataxia Fetal Growth Retardation Jaundice, Neonatal DiGeorge Syndrome Nervous System Diseases Heart Defects, Congenital Fragile X Syndrome Fetal Diseases Congenital Abnormalities Brain Diseases Chromosome Inversion Pregnancy Complications Disease Models, Animal Hypoglycemia Body Weight Genetic Predisposition to Disease

Chemicals and Drugs11

Potassium Channels, Inwardly Rectifying Sulfonylurea Receptors Anticonvulsants Codon, Nonsense Receptors, Drug Nerve Tissue Proteins Transcription Factors Proteins Genetic Markers Membrane Proteins DNA-Binding Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment49

Facies Comparative Genomic Hybridization Karyotyping In Situ Hybridization, Fluorescence Chromosome Banding Pedigree Cytogenetic Analysis Fluoridation Speech Therapy Magnetic Resonance Imaging Dental Care for Children Cohort Studies Chromosome Mapping Follow-Up Studies Neurologic Examination Electroencephalography Retrospective Studies DNA Mutational Analysis Questionnaires Mass Screening Case-Control Studies Risk Factors Delayed Diagnosis DMF Index Prenatal Diagnosis Disease Models, Animal Genetic Association Studies Oligonucleotide Array Sequence Analysis Cross-Sectional Studies Reproducibility of Results Analysis of Variance Physical Therapy Modalities Longitudinal Studies Treatment Outcome Prevalence Genetic Testing Statistics, Nonparametric Reference Values Body Height Body Weight Pregnancy Outcome Severity of Illness Index Prospective Studies Logistic Models Pilot Projects Polymerase Chain Reaction Prognosis Sensitivity and Specificity Sequence Analysis, DNA

Psychiatry and Psychology26

Developmental Disabilities Intellectual Disability Child Development Autistic Disorder Communication Disorders Psychomotor Disorders Child Development Disorders, Pervasive Regression (Psychology)Learning Disorders Motor Skills Child Behavior Disorders Parenting Social Behavior Motor Skills Disorders Intelligence Language Development Mother-Child Relations Mothers Psychomotor Performance Parents Family Child Behavior Attention Deficit Disorder with Hyperactivity Neuropsychological Tests Cognition Disorders Cognition

Phenomena and Processes69

Chromosome Duplication Child Development Chromosome Deletion Segmental Duplications, Genomic Phenotype Chromosomes, Human, Pair 15 Karyotype Tetrasomy Pregnancy Trisomy Chromosomes, Human, Pair 22 Consanguinity Mutation Chromosomes, Human, Pair 2 Haploinsufficiency Chromosomes, Human, Pair 16 Chromosome Breakage DNA Copy Number Variations Chromosomes, Human, Pair 1 Chromosome Aberrations Exome Sex Chromosome Aberrations Genes, Recessive Time Factors Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 13 Gene Duplication Homozygote Chromosomes, Human, X Chromosomes, Human, Pair 3 Gene Deletion Chromosomes, Human, Pair 4 Translocation, Genetic Gestational Age Chromosomes, Human, Pair 17 Mutation, Missense Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 12 Gene Dosage Heterozygote Chromosomes, Human, Pair 14 Mosaicism Psychomotor Performance Chromosomes, Human, Pair 7 Chromosome Inversion Embryonic Development Gene Expression Regulation, Developmental Codon, Nonsense Sequence Deletion Exons Chromosomes, Human, Pair 5 Larva Genotype Gene Rearrangement Base Sequence Embryonic and Fetal Development Body Height Body Weight Amino Acid Sequence Genetic Predisposition to Disease Aging Microsatellite Repeats Pregnancy Outcome Point Mutation Sensitivity and Specificity Polymorphism, Single Nucleotide Genetic Markers Sequence Homology, Amino Acid

Anthropology, Education, Sociology and Social Phenomena8

Education, Nonprofessional Play and Playthings Education, Special Mothers Parents Family Poverty Socioeconomic Factors

Humanities1

Information Science5

Questionnaires Molecular Sequence Data Base Sequence Prevalence Amino Acid Sequence

Named Groups5

Infant, Newborn Infant, Premature Mothers Parents Infant, Low Birth Weight

Health Care32

Early Intervention (Education)Fluoridation Dental Care for Children Cohort Studies Follow-Up Studies Maternal Exposure Retrospective Studies Questionnaires Mass Screening Case-Control Studies Family Health Risk Factors DMF Index Age of Onset Educational Status Cross-Sectional Studies Reproducibility of Results Age Factors Analysis of Variance Longitudinal Studies Treatment Outcome Prevalence Genetic Testing Poverty Statistics, Nonparametric Comorbidity Severity of Illness Index Prospective Studies Logistic Models Pilot Projects Socioeconomic Factors Sensitivity and Specificity

Geographicals2

California United States

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 Humanities Information Science Named Groups Health Care Geographicals

Developmental Disabilities Intellectual Disability Abnormalities, Multiple Microcephaly Muscle Hypotonia Syndrome Chromosome Duplication Early Intervention (Education)Child Development Autistic Disorder Chromosome Deletion Facies Failure to Thrive Craniofacial Abnormalities Language Development Disorders Infant, Newborn Growth Disorders Segmental Duplications, Genomic Comparative Genomic Hybridization Communication Disorders Phenotype Face Chromosome Disorders Karyotyping Chromosomes, Human, Pair 15 Karyotype Brain Diseases, Metabolic, Inborn Spasms, Infantile Agenesis of Corpus Callosum Osteopoikilosis Epilepsy Psychomotor Disorders In Situ Hybridization, Fluorescence Symbolism Tetrasomy Education, Nonprofessional Pregnancy Metabolism, Inborn Errors Nervous System Malformations Hand Deformities, Congenital Trisomy Chromosome Banding Pedigree Chromosomes, Human, Pair 22 Seizures Cerebral Palsy Child Development Disorders, Pervasive Consanguinity Mutation Asphyxia Neonatorum Angelman Syndrome Blepharophimosis Regression (Psychology)Craniosynostoses Eye Abnormalities Chromosomes, Human, Pair 2 Haploinsufficiency Learning Disorders Dwarfism Chromosomes, Human, Pair 16 Motor Skills Chromosome Breakage Prader-Willi Syndrome Kernicterus DNA Copy Number Variations Chromosomes, Human, Pair 1 Chromosome Aberrations Child Behavior Disorders Play and Playthings Exome Sex Chromosome Aberrations Cytogenetic Analysis Malformations of Cortical Development Prenatal Exposure Delayed Effects Genes, Recessive Time Factors Embryo Loss Infant, Premature, Diseases Purine-Pyrimidine Metabolism, Inborn Errors Fluoridation Chromosomes, Human, Pair 6 Foot Deformities, Congenital Chromosomes, Human, Pair 10 Speech Therapy Chromosomes, Human, Pair 13 Magnetic Resonance Imaging Gene Duplication Congenital Hypothyroidism Brain Neurocutaneous Syndromes De Lange Syndrome Abnormalities, Drug-Induced Parenting Coloboma Down Syndrome Homozygote Chromosomes, Human, X Dental Care for Children Chromosomes, Human, Pair 3 Infant, Premature

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