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A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2

Authors :
Maria Paola Canevini
Maurizio Elia
Maurizio De Fusco
Salvatore Striano
Rosanna Chifari
Renzo Guerrini
Pasquale Striano
Giorgio Casari
Striano, P
Chifari, R
Striano, Salvatore
DE FUSCO, M
Elia, M
Guerrini, R
Casari, G
Canevini, Mp
P., Striano
R., Chifari
M. d., Fusco
M., Elia
R., Guerrini
G., Casari
M. P., Canevini
Striano, S
de Fusco, M
Casari, GIORGIO NEVIO
Source :
Università degli studi di Firenze-IRIS
Publication Year :
2004
Publisher :
Lippincott, Williams & Wilkins:530 Walnut Street:Philadelphia, PA 19106:(800)638-3030, (301)223-2300, EMAIL: orders@lww.com, INTERNET: http://www.lww.com, Fax: (301)223-2320, (301)223-2320, 2004.

Abstract

Summary: 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.

Details

Language :
English
Database :
OpenAIRE
Journal :
Università degli studi di Firenze-IRIS
Accession number :
edsair.doi.dedup.....5bfb39f2a2115a7398f9e318873a1833