Autosomal Dominant Cortical Tremor, Myoclonus, and Epilepsy Syndrome mimicking Juvenile Myoclonic Epilepsy

Aydin Ozemir, ZeynepOguz Akarsu, EmelMatur, ZELİHAOge, Ali EmreBAYKAL, Betül2022-01-132022-01-132016-09-01Aydin Ozemir Z., Oguz Akarsu E., Matur Z., Oge A. E. , BAYKAL B., -Autosomal Dominant Cortical Tremor, Myoclonus, and Epilepsy Syndrome mimicking Juvenile Myoclonic Epilepsy-, NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, cilt.53, sa.3, ss.272-275, 2016http://hdl.handle.net/20.500.12645/30133Introduction: Autosomal dominant cortical tremor, myoclonus, and epilepsy (ADCME) syndrome is a genetically heterogeneous and under-recognized disease characterized by tremulous movements mimicking essential tremor, myoclonus, and rare generalized tonic-clonic seizures. Here we described the clinical and electrophysiological features of three siblings with ADCME syndrome mimicking juvenile myoclonic epilepsy (JME).info:eu-repo/semantics/openAccessAutosomal Dominant Cortical Tremor, Myoclonus, and Epilepsy Syndrome mimicking Juvenile Myoclonic EpilepsyArticleWOS:0003832547000158498337175810.5152/npa.2016.14841