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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Detalles Bibliográficos
Autores principales: Wong, Lee-Chin, Wu, Yen-Tzu, Hsu, Chia-Jui, Weng, Wen-Chin, Tsai, Wen-Che, Lee, Wang-Tso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611493/
https://www.ncbi.nlm.nih.gov/pubmed/31316448
http://dx.doi.org/10.3389/fneur.2019.00641

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611493/
https://www.ncbi.nlm.nih.gov/pubmed/31316448
http://dx.doi.org/10.3389/fneur.2019.00641

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