BRL43694A

\bˌiːˌɑːɹˈɛl fˈɔːtiθɹˈiː θˈa͡ʊzənd sˈɪkshˈʌndɹədən nˈa͡ɪntifˈɔːɹ ˈe͡ɪ], \bˌiːˌɑːɹˈɛl fˈɔːtiθɹˈiː θˈa‍ʊzənd sˈɪkshˈʌndɹədən nˈa‍ɪntifˈɔːɹ ˈe‍ɪ], \b_ˌiː__ˌɑː_ɹ_ˈɛ_l f_ˈɔː_t_i_θ_ɹ_ˈiː θ_ˈaʊ_z_ə_n_d_ s_ˈɪ_k_s_h_ˈʌ_n_d_ɹ_ə_d_ə_n n_ˈaɪ_n_t_i_f_ˈɔː_ɹ ˈeɪ]\

Definitions of BRL43694A

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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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