Infants with hypotonia. Medical search. Frequent questions

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Anatomy8

Chromosomes, Human, X Chromosomes, Human, Pair 15 Milk, Human Chromosomes, Human, Pair 22 Face Chromosomes, Human, Pair 4 Brain Cerebellum

Diseases44

Muscle Hypotonia Abnormalities, Multiple Intellectual Disability Infant, Premature, Diseases Facies Syndrome Prader-Willi Syndrome Sudden Infant Death Myopathies, Structural, Congenital Infant, Newborn, Diseases Microcephaly Myopathies, Nemaline Ataxia Muscle Hypertonia Failure to Thrive Myopathy, Central Core Chromosome Deletion Psychomotor Disorders Mental Retardation, X-Linked Sex Chromosome Disorders Barth Syndrome Cytochrome-c Oxidase Deficiency Kidney Diseases, Cystic Oculocerebrorenal Syndrome Cerebellar Diseases Spinal Muscular Atrophies of Childhood Congenital Disorders of Glycosylation Amino Acid Metabolism, Inborn Errors Muscular Diseases Growth Disorders Chromosome Disorders Acidosis, Lactic Eye Abnormalities Seizures Birth Weight Cerebellar Ataxia Muscular Dystrophies Down Syndrome Brain Diseases Infant Nutrition Disorders Respiratory Distress Syndrome, Newborn Bronchopulmonary Dysplasia Translocation, Genetic Chromosome Aberrations

Chemicals and Drugs1

Succinate-Semialdehyde Dehydrogenase

Analytical, Diagnostic and Therapeutic Techniques and Equipment16

Facies Infant Mortality Pedigree Bottle Feeding In Situ Hybridization, Fluorescence Karyotyping Comparative Genomic Hybridization Birth Weight Fatal Outcome Chromosome Banding Magnetic Resonance Imaging Intensive Care, Neonatal DNA Mutational Analysis Incubators, Infant Electromyography Infant Equipment

Psychiatry and Psychology9

Intellectual Disability Infant Behavior Developmental Disabilities Psychomotor Disorders Breast Feeding Child Development Bottle Feeding Crying Mothers

Phenomena and Processes21

Infant Nutritional Physiological Phenomena Chromosomes, Human, X Chromosome Deletion Consanguinity Breast Feeding Pregnancy Chromosomes, Human, Pair 15 Phenotype Child Development Genes, Recessive Gestational Age Chromosomes, Human, Pair 22 Birth Weight Mutation Mutation, Missense Muscle Tonus Homozygote Chromosomes, Human, Pair 4 Gene Duplication Translocation, Genetic Chromosome Aberrations

Anthropology, Education, Sociology and Social Phenomena2

Infant Welfare Mothers

Technology, Industry, Agriculture3

Infant Food Infant Formula Milk, Human

Information Science2

Infant Mortality Fatal Outcome

Named Groups8

Infant, Newborn Infant, Premature Infant, Very Low Birth Weight Infant, Low Birth Weight Infant, Extremely Low Birth Weight Infant, Extremely Premature Infant, Small for Gestational Age Mothers

Health Care6

Infant Care Infant Mortality Intensive Care Units, Neonatal Fatal Outcome Infectious Disease Transmission, Vertical Intensive Care, Neonatal

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

Muscle Hypotonia Infant, Newborn Infant, Premature Abnormalities, Multiple Intellectual Disability Infant, Premature, Diseases Infant Care Infant Food Facies Syndrome Prader-Willi Syndrome Infant Formula Infant Behavior Developmental Disabilities Infant Mortality Sudden Infant Death Myopathies, Structural, Congenital Infant, Newborn, Diseases Infant Nutritional Physiological Phenomena Microcephaly Myopathies, Nemaline Infant, Very Low Birth Weight Ataxia Muscle Hypertonia Infant, Low Birth Weight Failure to Thrive Chromosomes, Human, X Myopathy, Central Core Chromosome Deletion Psychomotor Disorders Mental Retardation, X-Linked Consanguinity Breast Feeding Infant Welfare Sex Chromosome Disorders Pedigree Barth Syndrome Pregnancy Cytochrome-c Oxidase Deficiency Chromosomes, Human, Pair 15 Kidney Diseases, Cystic Oculocerebrorenal Syndrome Cerebellar Diseases Infant, Extremely Low Birth Weight Phenotype Spinal Muscular Atrophies of Childhood Succinate-Semialdehyde Dehydrogenase Child Development Congenital Disorders of Glycosylation Milk, Human Genes, Recessive Gestational Age Amino Acid Metabolism, Inborn Errors Chromosomes, Human, Pair 22 Muscular Diseases Infant, Extremely Premature Growth Disorders Infant, Small for Gestational Age Chromosome Disorders Face Acidosis, Lactic Bottle Feeding Eye Abnormalities In Situ Hybridization, Fluorescence Seizures Karyotyping Comparative Genomic Hybridization Birth Weight Mutation Intensive Care Units, Neonatal Cerebellar Ataxia Crying Mutation, Missense Fatal Outcome Muscular Dystrophies Muscle Tonus Down Syndrome Homozygote Mothers Chromosomes, Human, Pair 4 Brain Diseases Gene Duplication Infant Nutrition Disorders Brain Respiratory Distress Syndrome, Newborn Bronchopulmonary Dysplasia Chromosome Banding Magnetic Resonance Imaging Infectious Disease Transmission, Vertical Translocation, Genetic Intensive Care, Neonatal DNA Mutational Analysis Chromosome Aberrations Incubators, Infant Electromyography Cerebellum Infant Equipment

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