MYOCLONIC ENCEPHALOPATHY
\mˌa͡ɪəklˈɒnɪk ɛnsˌɛfɐlˈɒpəθɪ], \mˌaɪəklˈɒnɪk ɛnsˌɛfɐlˈɒpəθɪ], \m_ˌaɪ_ə_k_l_ˈɒ_n_ɪ_k ɛ_n_s_ˌɛ_f_ɐ_l_ˈɒ_p_ə_θ_ɪ]\
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A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic (i.e., occurring secondary to known disease processes such as infections, hypoxic-ischemic injuries, trauma, etc.).
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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.
Nearby Words
- myoclonic astatic epilepsies
- myoclonic astatic epilepsy
- myoclonic cerebellar dyssynergia
- myoclonic cerebellar dyssynergias
- myoclonic encephalopathies
- Myoclonic Encephalopathy
- myoclonic epilepsies
- myoclonic epilepsy
- myoclonic epilepsy and ragged red fibers
- myoclonic epilepsy with ragged red fibers
- myoclonic epilepsy, early childhood