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A Challenging Diagnosis of Atypical Glut1-DS: A Case Report and Literature Review

Glucose transporter type 1 deficiency syndrome (Glut1-DS) is a rare neurometabolic disorder caused by mutations of the SLC2A1 gene. Paroxysmal exercise-induced dyskinesia is regarded as a representative symptom of Glut1-DS. Paroxysmal non-kinesigenic dyskinesia is usually caused by aberrations of th...

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Detalles Bibliográficos
Autores principales:	Yu, Miaomiao, Miao, Jing, Lv, Yudan, Wang, Xue, Zhang, Wuqiong, Shao, Na, Meng, Hongmei
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Neurology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876440/ https://www.ncbi.nlm.nih.gov/pubmed/33584489 http://dx.doi.org/10.3389/fneur.2020.549331

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