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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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| Publicado no: | Neurology |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5405761/ https://ncbi.nlm.nih.gov/pubmed/28341645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000003867 |
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