CENTRALOPATHIC EPILEPSIES
\sˌɛntɹɐləpˈaθɪk ˈɛpɪlˌɛpsɪz], \sˌɛntɹɐləpˈaθɪk ˈɛpɪlˌɛpsɪz], \s_ˌɛ_n_t_ɹ_ɐ_l_ə_p_ˈa_θ_ɪ_k ˈɛ_p_ɪ_l_ˌɛ_p_s_ɪ_z]\
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An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and dysarthria. The episodes tend to occur at night and may become secondarily generalized. In most cases, affected children are neurologically and developmentally normal. The electroencephalogram shows characteristic high-voltage sharp waves over the central temporal regions, which are more prominent during drowsiness and sleep. In general, seizures do not continue beyond mid-adolescence. (From Epilepsia 1998 39;Suppl 4:S32-S41)
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Word of the day
Dopamine Acetyltransferase
- An enzyme that catalyzes the of groups from acetyl-CoA to arylamines. They have wide specificity for aromatic amines, particularly serotonin, and can also catalyze acetyl transfer between arylamines without CoA. EC 2.3.1.5.