MARIES CEREBELLAR ATAXIA
\mˈe͡əɹiz sˈɛɹɪbˌɛləɹ atˈe͡ɪksi͡ə], \mˈeəɹiz sˈɛɹɪbˌɛləɹ atˈeɪksiə], \m_ˈeə_ɹ_i_z s_ˈɛ_ɹ_ɪ_b_ˌɛ_l_ə_ɹ a_t_ˈeɪ_k_s_iə]\
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A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked.
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