Challenges in deep brain stimulation for DYT-11: a single center troubleshooting experience
IntroductionDYT-11 is a form of myoclonus dystonia (MD) characterized by involuntary muscle jerks and abnormal postures attributable to a variant in the epsilon sarcoglycan (SGCE) gene. Treatment with pallidal deep brain stimulation (GPi-DBS) is effective, but prior studies have highlighted brisk an...
Saved in:
| Main Authors: | Matthew Aaron Remz, Vedant Garg, Kara A. Johnson, Ka Loong Kelvin Au, Abbas Babajani-Feremi, Venkat Srikar Lavu, Coralie de Hemptinne, Joshua K. Wong |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2025-07-01
|
| Series: | Dystonia |
| Subjects: | |
| Online Access: | https://www.frontierspartnerships.org/articles/10.3389/dyst.2025.14485/full |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Myoclonus-Dystonia Syndrome
by: J Gordon Millichap
Published: (2002-11-01) -
How can neurophysiological studies help with movement disorders characterization in clinical practice? A review
by: Talyta GRIPPE, et al. -
Myoclonus-Dystonia Syndrome and E-Sarcoglycan Deficiency
by: J Gordon Millichap
Published: (2002-10-01) -
Myoclonic status epilepticus with dystonia-like symptoms in patients with dementia: Report of two cases
by: Rosario V. Rossi, et al.
Published: (2025-03-01) -
Case report: Effective globus pallidus internus deep brain stimulation for patient with stiff-person syndrome
by: Ahmed Mohamed, et al.
Published: (2024-12-01)