FAMILIAL SPINOCEREBELLAR DEGENERATIONS
\famˈɪlɪəl spˈɪnə͡ʊsɹˌɛbɛlə dɪd͡ʒˌɛnəɹˈe͡ɪʃənz], \famˈɪlɪəl spˈɪnəʊsɹˌɛbɛlə dɪdʒˌɛnəɹˈeɪʃənz], \f_a_m_ˈɪ_l_ɪ__ə_l s_p_ˈɪ_n_əʊ_s_ɹ_ˌɛ_b_ɛ_l_ə d_ɪ_dʒ_ˌɛ_n_ə_ɹ_ˈeɪ_ʃ_ə_n_z]\
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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.
By DataStellar Co., Ltd
Nearby Words
- familial polyposis syndromes
- familial progressive myoclonic epilepsy
- familial retinoblastoma
- familial retinoblastomas
- familial spinocerebellar degeneration
- Familial Spinocerebellar Degenerations
- familial tonic clonic epilepsies
- familial tonic clonic epilepsy
- familial tremor
- familial tremors
- familiar