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...

Descripción completa

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

Internet

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

Ejemplares similares