STOMOXYS CALCITRANS

\stˈɒmɒksɪz kˈalsɪtɹˌanz], \stˈɒmɒksɪz kˈalsɪtɹˌanz], \s_t_ˈɒ_m_ɒ_k_s_ɪ_z k_ˈa_l_s_ɪ_t_ɹ_ˌa_n_z]\
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2010 - Medical Dictionary Database
By DataStellar Co., Ltd
 
1916 - Appleton's medical dictionary
By Smith Ely Jelliffe

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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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