Syndrome are cerebellar ataxia. Medical search. Frequent questions

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Anatomy3

Cerebellum Purkinje Cells Chromosomes, Human, Pair 19

Diseases31

Cerebellar Ataxia Ataxia Syndrome Spinocerebellar Ataxias Spinocerebellar Degenerations Friedreich Ataxia Gait Ataxia Ataxia Telangiectasia Stiff-Person Syndrome Olivopontocerebellar Atrophies Cerebellar Diseases Myoclonic Cerebellar Dyssynergia Reflex, Abnormal Down Syndrome Apraxias Machado-Joseph Disease Metabolic Syndrome X Nystagmus, Pathologic Foot Deformities Intellectual Disability Abnormalities, Multiple Multiple System Atrophy Ocular Motility Disorders Ophthalmoplegia Atrophy Dysarthria Paraneoplastic Cerebellar Degeneration Turner Syndrome Nephrotic Syndrome Optic Atrophy Anticipation, Genetic

Chemicals and Drugs4

Bromisovalum Ataxia Telangiectasia Mutated Proteins Gliadin Glutamate Decarboxylase

Analytical, Diagnostic and Therapeutic Techniques and Equipment3

Pedigree Reflex, Abnormal Magnetic Resonance Imaging

Psychiatry and Psychology2

Apraxias Intellectual Disability

Phenomena and Processes13

Genes, Recessive Reflex, Abnormal Genes, Dominant Mutation Trinucleotide Repeats Phenotype Trinucleotide Repeat Expansion Mutation, Missense Chromosomes, Human, Pair 19 Genetic Linkage Consanguinity Anticipation, Genetic Homozygote

Health Care1

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Health Care

Cerebellar Ataxia Ataxia Syndrome Spinocerebellar Ataxias Spinocerebellar Degenerations Friedreich Ataxia Gait Ataxia Ataxia Telangiectasia Pedigree Genes, Recessive Cerebellum Stiff-Person Syndrome Olivopontocerebellar Atrophies Cerebellar Diseases Myoclonic Cerebellar Dyssynergia Reflex, Abnormal Down Syndrome Age of Onset Apraxias Genes, Dominant Machado-Joseph Disease Metabolic Syndrome X Magnetic Resonance Imaging Purkinje Cells Mutation Trinucleotide Repeats Bromisovalum Nystagmus, Pathologic Foot Deformities Intellectual Disability Abnormalities, Multiple Phenotype Multiple System Atrophy Ocular Motility Disorders Ataxia Telangiectasia Mutated Proteins Ophthalmoplegia Gliadin Trinucleotide Repeat Expansion Atrophy Glutamate Decarboxylase Dysarthria Paraneoplastic Cerebellar Degeneration Mutation, Missense Chromosomes, Human, Pair 19 Turner Syndrome Nephrotic Syndrome Optic Atrophy Genetic Linkage Consanguinity Anticipation, Genetic Homozygote

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