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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Bibliografski detalji
Izdano u:Front Neurol
Glavni autori: Wong, Lee-Chin, Wu, Yen-Tzu, Hsu, Chia-Jui, Weng, Wen-Chin, Tsai, Wen-Che, Lee, Wang-Tso
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2019
Teme:
Neurology
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6611493/
https://ncbi.nlm.nih.gov/pubmed/31316448
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2019.00641
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