JONATHAN FALCONBRIDGE KELLY
\d͡ʒˈɒnəθən fˈalkənbɹˌɪd͡ʒ kˈɛli], \dʒˈɒnəθən fˈalkənbɹˌɪdʒ kˈɛli], \dʒ_ˈɒ_n_ə_θ_ə_n f_ˈa_l_k_ə_n_b_ɹ_ˌɪ_dʒ k_ˈɛ_l_i]\
Word of the day
Olivopontocerebellar Atrophies
- group inherited disorders which share progressive ataxia combination with atrophy CEREBELLUM; PONS; inferior olivary nuclei. Additional features include RIGIDITY; NYSTAGMUS; RETINAL DEGENERATION; MUSCLE SPASTICITY; DEMENTIA; URINARY INCONTINENCE; OPHTHALMOPLEGIA. familial has an earlier onset (second decade) and may feature spinal cord atrophy. sporadic form tends to present in the fifth or sixth decade, is considered a clinical subtype MULTIPLE SYSTEM ATROPHY. (From Adams et al., Principles of Neurology, 6th ed, p1085)
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