DOMINANTLY INHERITED SPINOCEREBELLAR ATAXIAS
\dˈɒmɪnəntli ɪnhˈɛɹɪtɪd spˈɪnə͡ʊsɹˌɛbɛləɹ atˈe͡ɪksi͡əz], \dˈɒmɪnəntli ɪnhˈɛɹɪtɪd spˈɪnəʊsɹˌɛbɛləɹ atˈeɪksiəz], \d_ˈɒ_m_ɪ_n_ə_n_t_l_i_ ɪ_n_h_ˈɛ_ɹ_ɪ_t_ɪ_d s_p_ˈɪ_n_əʊ_s_ɹ_ˌɛ_b_ɛ_l_ə_ɹ a_t_ˈeɪ_k_s_iə_z]\
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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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Proto Oncogene Proteins c erbB 2
- cell surface protein-tyrosine kinase that is found to be overexpressed in significant number adenocarcinomas. It has extensive homology can heterodimerize EGF EPIDERMAL GROWTH FACTOR), 3 receptor (RECEPTOR, 3) and the 4 receptor. Activation of erbB-2 receptor occurs during heterodimer formation with a ligand-bound erbB family members. EC 2.7.11.-.
Nearby Words
- dominant optic atrophies
- dominant optic atrophy
- dominant tenement
- dominantly
- dominantly inherited spinocerebellar ataxia
- Dominantly Inherited Spinocerebellar Ataxias
- dominarum aqua
- dominate
- dominated
- dominated by
- dominating