Ontology highlight
ABSTRACT:
SUBMITTER: Horisawa S
PROVIDER: S-EPMC7545596 | biostudies-literature | 2020 Oct
REPOSITORIES: biostudies-literature

Annals of clinical and translational neurology 20200904 10
Mutations in the lysine methyltransferase 2B (KMT2B) gene have recently been reported to be associated with childhood-onset generalized dystonia. There have been no studies investigating ablative treatments for the management of this disorder. Three patients underwent either a staged unilateral pallidotomy and contralateral pallidothalamic tractotomy (19-year-old man, 2-year follow-up), a unilateral pallidothalamic tractotomy (34-year-old man, 6-month follow-up) or a simultaneous unilateral pall ...[more]