Autosomal dominant cerebellar ataxia type I: A review of the phenotypic and genotypic characteristics

Medicine & Life Sciences

• Cerebellar Ataxia 100%
• Spinocerebellar Ataxias 89%
• Ataxia 70%
• Progressive Myoclonic Epilepsy 40%
• Dysarthria 33%
• Trinucleotide Repeat Expansion 20%
• Gait Ataxia 19%
• Founder Effect 18%
• Speech Therapy 17%
• Inheritance Patterns 17%
• Spinal Nerves 16%
• Occupational Therapy 15%
• Sequence Deletion 15%
• Nonsense Codon 15%
• Genetic Counseling 14%
• Gene Deletion 14%
• Peripheral Nervous System 14%
• Peripheral Nervous System Diseases 14%
• Missense Mutation 13%
• Genetic Testing 13%
• Neurologic Manifestations 13%
• Human Body 12%
• Open Reading Frames 12%
• Gait 12%
• Infections 12%
• Malnutrition 12%
• Neurodegenerative Diseases 11%
• Physical Examination 11%
• Cognitive Dysfunction 10%
• Spinal Cord 10%
• Disease Progression 10%
• Accidental Falls 10%
• Seizures 10%
• Differential Diagnosis 10%
• Poisons 9%
• Psychiatry 9%
• Pharmaceutical Preparations 5%
• Genes 5%
• Population 5%
• Therapeutics 4%