MARY ELIZABETH BRADDON

\mˈe͡əɹi ɪlˈɪzəbəθ bɹˈadən], \mˈe‍əɹi ɪlˈɪzəbəθ bɹˈadən], \m_ˈeə_ɹ_i_ ɪ_l_ˈɪ_z_ə_b_ə_θ b_ɹ_ˈa_d_ə_n]\

Definitions of MARY ELIZABETH BRADDON

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1910 - Warner's dictionary of authors ancient and modern
By Charles Dudley Warner

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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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