Back to Search
Start Over
A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2
- 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.
- Subjects :
- Adult
Male
Benign adult familial myoclonic epilepsy
classification/genetics
Genetic Linkage
Adult, Aged, Chromosomes
Human
Pair 2, Epilepsies
Myoclonic
classification/genetics, Family Health, Female, Genetic Linkage, Humans, Male, Pedigree, Phenotype
Epilepsies, Myoclonic
Epilepsies
Biology
Chromosomes
Epilepsy
Genetic linkage
medicine
Humans
Aged
Genetics
Linkage (software)
Family Health
Pair 2, Epilepsie
Genetic heterogeneity
Chromosome
Adult, Aged, Chromosome
medicine.disease
Phenotype
Pedigree
Neurology
Chromosomes, Human, Pair 2
Pair 2
Myoclonic epilepsy
Female
Neurology (clinical)
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Università degli studi di Firenze-IRIS
- Accession number :
- edsair.doi.dedup.....5bfb39f2a2115a7398f9e318873a1833