A case of sensory ataxic neuropathy, dysarthria, and ophthalmoparesis with multiple mitochondrial DNA deletions

Medicine and Dentistry

• Dysarthria 100%
• Ophthalmoparesis 100%
• Neuropathy 80%
• Muscle 80%
• Muscle Weakness 60%
• Lactic Acid 60%
• Mitochondrial DNA 60%
• Exon 60%
• Age 40%
• Serum 40%
• Pyruvic Acid 40%
• Atrophy 40%
• Leg 40%
• Basal Ganglia 40%
• Sural Nerve 40%
• Brain 40%
• Peripheral Nerve 40%
• Ptosis 40%
• Nerve Biopsy 40%
• Patient 20%
• Gene 20%
• Biopsy 20%
• Man 20%
• Lesion 20%
• Limb 20%
• Magnetic Resonance Imaging 20%
• Hearing Impairment 20%
• Head 20%
• Neurologic Examination 20%
• Aerobic Exercise 20%
• Plummer-Vinson Syndrome 20%
• Cause of Death 20%
• Electromyography 20%
• Gait 20%
• Weakness 20%
• Sensation 20%
• Cytochrome C 20%
• DeJerine-Sottas Disease 20%
• Sensorineural Hearing Loss 20%
• Nerve Conduction 20%
• Sensory Ataxia 20%
• Cerebrospinal Fluid 20%
• Exercise Test 20%
• Untranslated Region 20%
• Point Mutation 20%
• Fibrillation 20%
• Nerve Conduction Study 20%
• F Wave 20%
• Genetic Screening 20%

Neuroscience

• Dysarthria 100%
• Peripheral Neuropathy 80%
• Exon 60%
• Mitochondrial DNA 60%
• Sural Nerve 40%
• Gene 20%
• Magnetic Resonance Imaging 20%
• Ataxia 20%
• Electromyography 20%
• Nerve Conduction 20%
• Untranslated Region 20%
• Gait 20%
• Charcot-Marie-Tooth Disease 20%
• Cytochrome C 20%
• Point Mutation 20%
• Nerve Conduction Study 20%
• Sensation of Hearing 20%
• Sensorineural Hearing Loss 20%