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Linkage of familial essential tremor to chromosome 5q35.

Authors :
Hicks, James E.
Konidari, Ioanna
Scott, Burton L.
Stajich, Jeffrey M.
Ashley‐Koch, Allison E.
Gilbert, John R.
Scott, William K.
Ashley-Koch, Allison E
Source :
Movement Disorders. Jul2016, Vol. 31 Issue 7, p1059-1062. 4p.
Publication Year :
2016

Abstract

<bold>Background: </bold>Essential tremor is a neurological condition characterized by tremor during voluntary movement. To date, 3 loci linked to familial essential tremor have been identified.<bold>Methods: </bold>We examined 48 essential tremor patients in 5 large essential tremor pedigrees in our data set for genetic linkage using an Affymetrix Axiom array. Linkage analysis was performed using an affecteds-only dominant model in SIMWALK2. To incorporate all genotype information, GERMLINE was used to identify genome segments shared identical-by-descent in pairs of affecteds. Exome sequencing was performed in pedigrees showing evidence of linkage.<bold>Results: </bold>For one family, chromosomes 5 and 18 showed genome-wide significant linkage to essential tremor. Shared segment analysis excluded the 18p11 candidate region and reduced the 5q35 region by 1 megabase. Exome sequencing did not identify a potential causative variant in this region.<bold>Conclusion: </bold>A locus on chromosome 5 is linked to essential tremor. Further research is needed to identify a causative variant. © 2016 International Parkinson and Movement Disorder Society. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08853185
Volume :
31
Issue :
7
Database :
Academic Search Index
Journal :
Movement Disorders
Publication Type :
Academic Journal
Accession number :
116620122
Full Text :
https://doi.org/10.1002/mds.26582