Severe Pediatric Dystonia Responding to Deep Brain Stimulation in 22q11.2 Microduplication Syndrome: Rare Clinical Presentation-Reference-Cited by-同舟云学术

Severe Pediatric Dystonia Responding to Deep Brain Stimulation in 22q11.2 Microduplication Syndrome: Rare Clinical Presentation

Published:2024-01-09 Issue: Volume: Page:
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Movement Disord Clin Pract

Author:

AlGethami Hanin Jaber¹²,Breitbart Sara³,Warsi Nebras M.³⁴,Fasano Alfonso¹⁵⁶⁷⁸,Ibrahim George M.³⁴⁹,Gorodetsky Carolina¹²^ORCID

Affiliation:

1. Division of Neurology The Hospital for Sick Children Toronto Ontario Canada

2. Department of Pediatrics University of Toronto Toronto Ontario Canada

3. Division of Neurosurgery The Hospital for Sick Children Toronto Ontario Canada

4. Department of Surgery University of Toronto Toronto Ontario Canada

5. Edmond J. Safra Program in Parkinson's Disease, Morton and Gloria Shulman Movement Disorders Clinic, Toronto Western Hospital, UHN Toronto Ontario Canada

6. Division of Neurology University of Toronto Toronto Ontario Canada

7. Krembil Brain Institute Toronto Ontario Canada

8. CenteR for Advancing Neurotechnological Innovation to Application (CRANIA) Toronto Ontario Canada

9. Institute of Biomedical Engineering, University of Toronto Toronto Ontario Canada

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference10 articles.

1. The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplication

2. Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

3. The Burke-Fahn-Marsden Dystonia Rating Scale is Age-Dependent in Healthy Children

4. Pediatric Quality of Life InventoryTM version 4.0 short form generic core scale across pediatric populations review data

5. Lead-DBS v2: Towards a comprehensive pipeline for deep brain stimulation imaging