Cognition and Evolution of Movement Disorders of FOXG1-Related Syndrome

FOXG1-related syndrome is a rare neurodevelopmental encephalopathy characterized by early onset hyperkinetic movement disorders, absent language, autistic features, epilepsy, and severe cognitive impairment. However, detailed evaluation of cognition and evolution of movement disorders over time have...

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Bibliographic Details
Main Authors: Lee-Chin Wong, Yen-Tzu Wu, Chia-Jui Hsu, Wen-Chin Weng, Wen-Che Tsai, Wang-Tso Lee
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-06-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2019.00641/full