Clinical differences between early and adult onset. Medical search. Frequent questions

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Anatomy1

Organisms1

Diseases21

Still's Disease, Adult-Onset Chronic Disease Dystonia Musculorum Deformans Dystonia Mastocytoma, Skin Epilepsy, Tonic-Clonic Epilepsies, Myoclonic Muscle Cramp Torticollis Epilepsy, Generalized Myotonic Dystrophy Pantothenate Kinase-Associated Neurodegeneration Arthritis, Juvenile Syndrome Coma Dermatomyositis Muscular Diseases Myositis Huntington Disease Genetic Predisposition to Disease Disease Models, Animal

Chemicals and Drugs3

HLA-B39 Antigen Hexosaminidase A Oxazoles

Analytical, Diagnostic and Therapeutic Techniques and Equipment13

Treatment Outcome Severity of Illness Index Retrospective Studies Prospective Studies Follow-Up Studies Risk Factors Prognosis Pedigree Magnetic Resonance Imaging Electroencephalography Case-Control Studies Disease Models, Animal Tomography, X-Ray Computed

Psychiatry and Psychology1

Huntington Disease

Phenomena and Processes11

Phenotype Genes, Dominant Genetic Linkage Mutation Epigenesis, Genetic Genes, Recessive Genetic Predisposition to Disease Genotype Pregnancy Time Factors Labor Onset

Information Science1

Molecular Sequence Data

Health Care9

Age of Onset Treatment Outcome Severity of Illness Index Retrospective Studies Prospective Studies Follow-Up Studies Risk Factors Age Factors Case-Control Studies

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

Still's Disease, Adult-Onset Age of Onset Treatment Outcome Severity of Illness Index Retrospective Studies Phenotype Prospective Studies Chronic Disease Follow-Up Studies Risk Factors Dystonia Musculorum Deformans Prognosis Dystonia Mastocytoma, Skin Morbillivirus Epilepsy, Tonic-Clonic Epilepsies, Myoclonic Muscle Cramp HLA-B39 Antigen Pedigree Torticollis Hexosaminidase A Epilepsy, Generalized Myotonic Dystrophy Pantothenate Kinase-Associated Neurodegeneration Arthritis, Juvenile Syndrome Coma Oxazoles Dermatomyositis Genes, Dominant Muscular Diseases Myositis Genetic Linkage Mutation Magnetic Resonance Imaging Epigenesis, Genetic Genes, Recessive Age Factors Huntington Disease Genetic Predisposition to Disease Electroencephalography Brain Case-Control Studies Genotype Pregnancy Disease Models, Animal Tomography, X-Ray Computed Molecular Sequence Data Time Factors Labor Onset

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