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Abnormal gait and hypoglycorrhachia in a toddler with seizures

INTRODUCTION: Glucose transporter type 1 (Glut1) deficiency syndrome is a treatable neurometabolic disorder characterized by seizures, developmental delay, and hypoglycorrhachia. Due to the rareness and non‐specific clinical manifestations, it is usually mis‐ or underdiagnosed. CASE PRESENTATION: We...

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Detalles Bibliográficos
Autores principales:	Angeli, Maria, Vergadi, Eleni, Niotakis, Georgios, Raissaki, Maria, Galanakis, Emmanouil
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2022
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960915/ https://www.ncbi.nlm.nih.gov/pubmed/35382425 http://dx.doi.org/10.1002/ped4.12311

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