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Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ε-sarcoglycan mutations.

Authors :
Raymond, Deborah
Saunders-Pullman, Rachel
de Carvalho Aguiar, Patricia
Schule, Birgitt
Kock, Norman
Friedman, Jennifer
Harris, Juliette
Ford, Blair
Frucht, Steven
Heiman, Gary A.
Jennings, Danna
Doheny, Dana
Brin, Mitchell F.
de Leon Brin, Deborah
Multhaupt-Buell, Trisha
Lang, Anthony E.
Kurlan, Roger
Klein, Christine
Ozelius, Laurie
Bressman, Susan
Source :
Movement Disorders. Mar2008, Vol. 23 Issue 4, p588-592. 5p.
Publication Year :
2008

Abstract

Myoclonus-dystonia (M-D) due to SGCE mutations is characterized by early onset myoclonic jerks, often associated with dystonia. Penetrance is influenced by parental sex, but other sex effects have not been established. In 42 affected individuals from 11 families with identified mutations, we found that sex was highly associated with age at onset regardless of mutation type; the median age onset for girls was 5 years versus 8 years for boys ( P < 0.0097). We found no association between mutation type and phenotype. © 2007 Movement Disorder Society [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
08853185
Volume :
23
Issue :
4
Database :
Academic Search Index
Journal :
Movement Disorders
Publication Type :
Academic Journal
Accession number :
64243038
Full Text :
https://doi.org/10.1002/mds.21785