Pre-eminent 20th-century American neurologist (1872-1937) who described a number of important diseases.
Including:
Ramsay Hunt paralysis: An hereditary disorder resembling adult Parkinson's disease, but less severe, characterized by myoclonus and signs of cerebellar dysfunction, especially intention tremor and ataxia. Mental functions are intact. Due to degeneration of the globus pallidus. Onset between the ages of 10 and 30 years. Inheritance is autosomal dominant. Described by Ramsay Hunt in 1917.
Ramsay Hunt syndrome I: A disorder characterized by myoclonus and signs of cerebellar dysfunction, especially intention tremor and ataxia, and occasional tonic-clonic seizures. Also known as myoclonus and ataxia. Described by Ramsay Hunt in 1921.
Ramsay Hunt syndrome II: This is far and away the best known syndrome associated with Ramsay Hunt's name. It is due to a herpes
virus infection of the geniculate nerve ganglion that causes paralysis of the facial muscles on the same side of the face as the infection. For more information, see: Ramsay Hunt syndrome.
Ramsay Hunt syndrome III: Occupational compression neuritis of the deep palmar branch of the ulnar nerve.
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