GNAO1 Mutation–Induced Pediatric Dystonic Storm Rescue With Pallidal Deep Brain Stimulation

Author:

Honey C. Michael1,Malhotra Armaan K.2,Tarailo-Graovac Maja3456,van Karnebeek Clara D. M.78,Horvath Gabriella49,Sulistyanto Adi10

Affiliation:

1. Department of Surgery, Section of Neurosurgery, University of Manitoba, Winnipeg, Canada

2. Faculty of Medicine, University of British Columbia, Vancouver, Canada

3. Centre for Molecular Medicine and Therapeutics, Vancouver, Canada

4. BC Children’s Hospital Research Institute, University of British Columbia, Vancouver, Canada

5. Department of Medical Genetics, University of British Columbia, Vancouver, Canada

6. Institute of Physiology and Biochemistry, Faculty of Biology, University of Belgrade, Belgrade, Serbia

7. Department of Pediatrics, BC Children’s Hospital Research Institute, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, Canada

8. Department of Pediatrics, Emma Children’s Hospital, Academic Medical Centre, Amsterdam, the Netherlands

9. Division of Biochemical Diseases, Department of Pediatrics, University of British Columbia, Vancouver, Canada

10. Division of Neurosurgery, Department of Surgery, University of British Columbia, Vancouver, Canada

Abstract

Dystonic storm or status dystonicus is a life-threatening hyperkinetic movement disorder with biochemical alterations due to the excessive muscle contractions. The medical management can require pediatric intensive care unit admission and a combination of medications while the underlying trigger is managed. Severe cases may require general anesthesia and paralytic agents with intubation and may relapse when these drugs are weaned. Deep brain stimulation of the globus pallidum has been reported to terminate dystonic storm in several pediatric cases. We present a 10-year-old boy with a de novo GNAO1 mutation–induced dystonic storm who required a 2-month pediatric intensive care unit admission and remained refractory to all medical treatments. Deep brain stimulation was performed under general anesthetic without complication. His dyskinetic movements stopped with initiation of stimulation. He was discharged from the pediatric intensive care unit after 4 days. We present prospectively evaluated changes in dystonia symptoms and quality of life for a patient with GNAO1 mutation treated with deep brain stimulation.

Publisher

SAGE Publications

Subject

Clinical Neurology,Pediatrics, Perinatology, and Child Health

Cited by 34 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3