Late onset deafness. Medical search. Frequent questions

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Anatomy22

Cochlea Ear, Inner Hair Cells, Auditory Spiral Ganglion Stria Vascularis Sural Nerve Brain Endolymph Cochlear Nerve Organ of Corti Hair Cells, Auditory, Inner Stereocilia Tectorial Membrane Stapes Vestibular Aqueduct Temporal Bone Cochlear Duct Hair Cells, Auditory, Outer Vestibule, Labyrinth Auditory Cortex Ear Cochlear Nucleus

Organisms3

Mice, Knockout Streptococcus agalactiae Mice, Transgenic

Diseases54

Deafness Hearing Loss, Sensorineural Hearing Loss Syndrome Cerebellar Ataxia Alzheimer Disease Hearing Loss, Unilateral Ornithine Carbamoyltransferase Deficiency Disease Hearing Loss, Bilateral Ataxia Osteochondrosis Genetic Predisposition to Disease Usher Syndromes Hearing Loss, Central Charcot-Marie-Tooth Disease Wolfram Syndrome Cerebrospinal Fluid Otorrhea Huntington Disease Spinocerebellar Degenerations Waardenburg Syndrome Hypoparathyroidism Jervell-Lange Nielsen Syndrome Cochlear Diseases Disease Models, Animal Vestibular Diseases Leukodystrophy, Metachromatic Glucose Metabolism Disorders Friedreich Ataxia Hearing Disorders Atrophy Sepsis Infant, Premature, Diseases Hearing Loss, Conductive Neuromuscular Diseases Labyrinth Diseases Abnormalities, Multiple Disease Progression Ichthyosis Goiter Gangliosidoses Nerve Degeneration Bulbar Palsy, Progressive Agammaglobulinemia Nephritis, Hereditary Nervous System Diseases Adrenal Hyperplasia, Congenital Tremor Coloboma Facial Paralysis Chromosome Disorders Parkinson Disease Cystitis Keratoderma, Palmoplantar Muscular Dystrophies

Chemicals and Drugs10

Connexins Myelin P0 Protein Apolipoproteins E DNA, Mitochondrial Transcription Factor Brn-3C Apolipoprotein E4 KCNQ Potassium Channels Membrane Proteins DNA Nerve Tissue Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment28

Pedigree DNA Mutational Analysis Cochlear Implants Audiometry Cochlear Implantation Genetic Testing Chromosome Mapping Heterozygote Detection Lipreading Hearing Tests Magnetic Resonance Imaging Retrospective Studies Risk Factors Sign Language Audiometry, Pure-Tone Severity of Illness Index Disease Models, Animal Case-Control Studies Polymerase Chain Reaction Follow-Up Studies Cohort Studies Acoustic Stimulation Treatment Outcome Prospective Studies Hearing Aids Incidence Neurologic Examination Fatal Outcome

Psychiatry and Psychology7

Alzheimer Disease Hearing Auditory Threshold Huntington Disease Sign Language Neuropsychological Tests Auditory Perception

Phenomena and Processes29

Genes, Recessive Mutation Phenotype Evoked Potentials, Auditory, Brain Stem Time Factors Genetic Linkage Hearing Alleles Genotype Genes, Dominant Heterozygote Homozygote Mutation, Missense Consanguinity Genetic Predisposition to Disease Lod Score Point Mutation Exons Haplotypes Gene Frequency Base Sequence Polymorphism, Genetic Hair Color Polymorphism, Single-Stranded Conformational Pregnancy Polymorphism, Single Nucleotide Amino Acid Sequence Aging Trinucleotide Repeats

Anthropology, Education, Sociology and Social Phenomena2

National Institute on Aging (U.S.)National Institute on Deafness and Other Communication Disorders (U.S.)

Information Science7

Lipreading Molecular Sequence Data Sign Language Base Sequence Amino Acid Sequence Incidence Fatal Outcome

Named Groups4

Infant, Newborn Persons With Hearing Impairments Infant, Very Low Birth Weight Infant, Premature

Health Care18

Age of Onset Age Factors Genetic Testing Retrospective Studies Family Health Risk Factors Intensive Care Units, Neonatal Severity of Illness Index Case-Control Studies National Institute on Aging (U.S.)Follow-Up Studies Cohort Studies Treatment Outcome Prospective Studies Incidence Sex Factors National Institute on Deafness and Other Communication Disorders (U.S.)Fatal Outcome

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

Deafness Age of Onset Hearing Loss, Sensorineural Pedigree Genes, Recessive Cochlea Hearing Loss Mutation Syndrome Cerebellar Ataxia Phenotype Ear, Inner Evoked Potentials, Auditory, Brain Stem Connexins Alzheimer Disease Hearing Loss, Unilateral Hair Cells, Auditory Time Factors DNA Mutational Analysis Genetic Linkage Spiral Ganglion Stria Vascularis Hearing Alleles Genotype Genes, Dominant Heterozygote Ornithine Carbamoyltransferase Deficiency Disease Cochlear Implants Audiometry Hearing Loss, Bilateral Homozygote Age Factors Infant, Newborn Mutation, Missense Consanguinity Ataxia Osteochondrosis Cochlear Implantation Genetic Testing Genetic Predisposition to Disease Usher Syndromes Chromosome Mapping Heterozygote Detection Sural Nerve Myelin P0 Protein Brain Lipreading Hearing Tests Hearing Loss, Central Magnetic Resonance Imaging Endolymph Molecular Sequence Data Retrospective Studies Lod Score Charcot-Marie-Tooth Disease Point Mutation Wolfram Syndrome Family Health Auditory Threshold Cochlear Nerve Exons Risk Factors Cerebrospinal Fluid Otorrhea Huntington Disease Spinocerebellar Degenerations Apolipoproteins E Organ of Corti Sign Language Waardenburg Syndrome Hypoparathyroidism Audiometry, Pure-Tone Hair Cells, Auditory, Inner Haplotypes DNA, Mitochondrial Gene Frequency Intensive Care Units, Neonatal Jervell-Lange Nielsen Syndrome Base Sequence Stereocilia Severity of Illness Index Cochlear Diseases Disease Models, Animal Tectorial Membrane Vestibular Diseases Leukodystrophy, Metachromatic Stapes Case-Control Studies Glucose Metabolism Disorders National Institute on Aging (U.S.)Friedreich Ataxia Transcription Factor Brn-3C Hearing Disorders Polymorphism, Genetic Atrophy Sepsis Polymerase Chain Reaction Apolipoprotein E4 Follow-Up Studies Infant, Premature, Diseases

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