Ontology highlight
ABSTRACT:
SUBMITTER: Peall KJ
PROVIDER: S-EPMC4052887 | biostudies-literature | 2013 Jan
REPOSITORIES: biostudies-literature
Peall Kathryn J KJ Smith Daniel J DJ Kurian Manju A MA Wardle Mark M Waite Adrian J AJ Hedderly Tammy T Lin Jean-Pierre JP Smith Martin M Whone Alan A Pall Hardev H White Cathy C Lux Andrew A Jardine Philip P Bajaj Narinder N Lynch Bryan B Kirov George G O'Riordan Sean S Samuel Michael M Lynch Timothy T King Mary D MD Chinnery Patrick F PF Warner Thomas T TT Blake Derek J DJ Owen Michael J MJ Morris Huw R HR
Brain : a journal of neurology 20130101 Pt 1
Myoclonus dystonia syndrome is a childhood onset hyperkinetic movement disorder characterized by predominant alcohol responsive upper body myoclonus and dystonia. A proportion of cases are due to mutations in the maternally imprinted SGCE gene. Previous studies have suggested that patients with SGCE mutations may have an increased rate of psychiatric disorders. We established a cohort of patients with myoclonus dystonia syndrome and SGCE mutations to determine the extent to which psychiatric dis ...[more]