Benign Adult Familial Myoclonic Epilepsy is an AD syndrome characterized from a non progressive cortical tremor resembling essential tremor, myoclonus and rare GTCS, first described from Japanese AA. Despite the different acronyms used (FEME, FCTE, BAFME, FAME), it seems to be a well definite clinical picture. Recently, non-Japanese families with similar phenotype, have been also described. We have already reported two, and recently observed a third, Italian families with linkage to chromosome 2p11.1-q12.2. In our opinion, this syndrome has a worldwide diffusion; it is genetically heterogeneous and might be overlooked.
FEME, FCTE, BAFME, FAME, ADCME,...: The spectrum of Benign Adult Familial Myoclonic Epilepsy: Review of Literature's cases
Striano P.;Zara F.;
2003-01-01
Abstract
Benign Adult Familial Myoclonic Epilepsy is an AD syndrome characterized from a non progressive cortical tremor resembling essential tremor, myoclonus and rare GTCS, first described from Japanese AA. Despite the different acronyms used (FEME, FCTE, BAFME, FAME), it seems to be a well definite clinical picture. Recently, non-Japanese families with similar phenotype, have been also described. We have already reported two, and recently observed a third, Italian families with linkage to chromosome 2p11.1-q12.2. In our opinion, this syndrome has a worldwide diffusion; it is genetically heterogeneous and might be overlooked.
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