VENAE VORTICOSAE

\vˈɛniː vˈɔːtɪkˌɒsiː], \vˈɛniː vˈɔːtɪkˌɒsiː], \v_ˈɛ_n_iː v_ˈɔː_t_ɪ_k_ˌɒ_s_iː]\

Definitions of VENAE VORTICOSAE

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1898 - American pocket medical dictionary
By Willam Alexander Newman Dorland

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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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