BENIGN CHILDHOOD EPILEPSY WITH CENTRO TEMPORAL SPIKES
\bɪnˈa͡ɪn t͡ʃˈa͡ɪldhʊd ˈɛpɪlˌɛpsi wɪð sˈɛntɹə͡ʊ tˈɛmpəɹə͡l spˈa͡ɪks], \bɪnˈaɪn tʃˈaɪldhʊd ˈɛpɪlˌɛpsi wɪð sˈɛntɹəʊ tˈɛmpəɹəl spˈaɪks], \b_ɪ_n_ˈaɪ_n tʃ_ˈaɪ_l_d_h_ʊ_d ˈɛ_p_ɪ_l_ˌɛ_p_s_i w_ɪ_ð s_ˈɛ_n_t_ɹ_əʊ t_ˈɛ_m_p_ə_ɹ_əl s_p_ˈaɪ_k_s]\
Definitions of BENIGN CHILDHOOD EPILEPSY WITH CENTRO TEMPORAL SPIKES
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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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Nearby Words
- benign
- benign brain neoplasm
- benign brain neoplasms
- benign cerebellar neoplasm
- benign cerebellar neoplasms
- Benign Childhood Epilepsy With Centro Temporal Spikes
- benign cranial nerve neoplasms
- benign cranial nerve tumors
- benign cranial neuroma
- benign cranial neuromas
- benign epilepsy, childhood, centrotemporal spikes