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

Internet

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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