Familial Cerebellar Degeneration with Slow Eye‐movements, Mental Deterioration and Incidental Nevus of Ota (Oculo‐dermal Melanoeytosis)

Keyphrases

• Incidental 100%
• Nevus 100%
• Eye Movements 100%
• Cerebellar Degeneration 100%
• Mental Deterioration 100%
• Nevus of Ota 100%
• Nystagmus 25%
• Pacientes 25%
• Literatur 16%
• Sein 16%
• Famille 16%
• Autosomal Dominant 8%
• Seizure 8%
• Neurological Diseases 8%
• Saccades 8%
• Successive Generations 8%
• Pontine 8%
• Reticularis 8%
• Reticle 8%
• Enfermedad 8%
• Maladies 8%
• Oculomotor Abnormalities 8%
• Embargo 8%
• Neurocutaneous Syndromes 8%
• Saccadic Movements 8%
• Epilepsia 8%
• Crise 8%
• Familia 8%
• Brainstem Lesion 8%
• Paramedian Pontine Reticular Formation 8%
• Anomala 8%
• Oculodermal Melanocytosis 8%
• Generaciones 8%
• Historia 8%
• Grand Mal Seizure 8%
• CadA 8%
• Histoire 8%
• TenA 8%
• Grand Mal 8%

Medicine and Dentistry

• Mental Deterioration 100%
• Nevus of Ota 100%
• Cerebellum Degeneration 100%
• Nevus 100%
• Saccadic Eye Movement 25%
• Grand Mal Epilepsy 25%
• Epileptic Seizure 12%
• Brainstem 12%
• Neurologic Disease 12%
• Autosomal Dominant Inheritance 12%
• Epilepsy 12%
• Reticular Formation 12%
• Phakomatosis 12%
• Melanocytosis 12%
• Chlorpheniramine Maleate 12%
• Ultralente 12%

Agricultural and Biological Sciences

• Nevus 100%
• Anomala 6%
• Reticular Formation 6%
• Brainstem 6%