Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by cortical tremor and generalized seizures, mapped on chromosome 8q24 by Japanese authors. Recently the same phenotype also was reported in European families, with linkage on chromosome 2. We present a new family with suggestion of linkage to chromosome 2p11.1-2q12.2 (lod score value, 1.55). This observation would confirm that BAFME is a worldwide, genetically heterogeneous condition, probably with Japanese families linked to 8q24 and European families to 2p11.1-q12.2
International audienceBACKGROUND: Familial cortical myoclonic tremor with epilepsy (FCMTE) is define...
Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characterized by dista...
Fourteen of the 26 members of two families with hereditary myoclonic epilepsy were studied, and the ...
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by...
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by...
Benign adult familial myoclonic epilepsy (BAFME) has been mapped to chromosome 8q24; however, geneti...
Benign adult familial myoclonic epilepsy (BAFME or FAME) is an autosomal dominant condition, charact...
Benign Adult Familial Myoclonic Epilepsy is an AD syndrome characterized from a non progressive cort...
SummaryBenign adult familial myoclonic epilepsy is an autosomal dominant idiopathic epileptic syndro...
Familial essential myoclonus and epilepsy (FEME) is hereditary epileptic disorder characterized by a...
Depienne and colleagues recently mapped to 5p15.31–p15 a French family with cortical tremor, myoclon...
In 1997, a locus for benign familial infantile convulsions (BFIC) was mapped to chromosome 19q. Furt...
Objectives To describe the clinical characteristics of a large Dutch family with cortical tremor wit...
Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder characterized by adul...
Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder characterized by adul...
International audienceBACKGROUND: Familial cortical myoclonic tremor with epilepsy (FCMTE) is define...
Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characterized by dista...
Fourteen of the 26 members of two families with hereditary myoclonic epilepsy were studied, and the ...
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by...
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant condition characterized by...
Benign adult familial myoclonic epilepsy (BAFME) has been mapped to chromosome 8q24; however, geneti...
Benign adult familial myoclonic epilepsy (BAFME or FAME) is an autosomal dominant condition, charact...
Benign Adult Familial Myoclonic Epilepsy is an AD syndrome characterized from a non progressive cort...
SummaryBenign adult familial myoclonic epilepsy is an autosomal dominant idiopathic epileptic syndro...
Familial essential myoclonus and epilepsy (FEME) is hereditary epileptic disorder characterized by a...
Depienne and colleagues recently mapped to 5p15.31–p15 a French family with cortical tremor, myoclon...
In 1997, a locus for benign familial infantile convulsions (BFIC) was mapped to chromosome 19q. Furt...
Objectives To describe the clinical characteristics of a large Dutch family with cortical tremor wit...
Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder characterized by adul...
Familial adult myoclonus epilepsy (FAME) is a rare autosomal dominant disorder characterized by adul...
International audienceBACKGROUND: Familial cortical myoclonic tremor with epilepsy (FCMTE) is define...
Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characterized by dista...
Fourteen of the 26 members of two families with hereditary myoclonic epilepsy were studied, and the ...