Paroxysmal eye–head movements in Glut1 deficiency syndrome

OBJECTIVE: To describe a characteristic paroxysmal eye–head movement disorder that occurs in infants with Glut1 deficiency syndrome (Glut1 DS). METHODS: We retrospectively reviewed the medical charts of 101 patients with Glut1 DS to obtain clinical data about episodic abnormal eye movements and anal...

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Detalles Bibliográficos
Autores principales: Pearson, Toni S., Pons, Roser, Engelstad, Kristin, Kane, Steven A., Goldberg, Michael E., De Vivo, Darryl C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405761/
https://www.ncbi.nlm.nih.gov/pubmed/28341645
http://dx.doi.org/10.1212/WNL.0000000000003867

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405761/
https://www.ncbi.nlm.nih.gov/pubmed/28341645
http://dx.doi.org/10.1212/WNL.0000000000003867

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