TYPE 1 SPINOCEREBELLAR ATAXIA
\tˈa͡ɪp wˈɒn spˈɪnə͡ʊsɹˌɛbɛləɹ atˈe͡ɪksi͡ə], \tˈaɪp wˈɒn spˈɪnəʊsɹˌɛbɛləɹ atˈeɪksiə], \t_ˈaɪ_p w_ˈɒ_n s_p_ˈɪ_n_əʊ_s_ɹ_ˌɛ_b_ɛ_l_ə_ɹ a_t_ˈeɪ_k_s_iə]\
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A group of dominantly inherited, predominantly late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57 (6):531-43)
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Word of the day
tinctura quininae ammoniata
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Nearby Words
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- Type 1 Spinocerebellar Ataxia
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- type 2 plasminogen activator inhibitor