Classic Ketogenic Diet and Modified Atkins Diet in SLC2A1 Positive and Negative Patients with Suspected GLUT1 Deficiency Syndrome: A Single Center Analysis of 18 Cases

Background: Glucose transporter type 1 deficiency syndrome (GLUT1DS) is caused by mutations in the SLC2A1 gene and produces seizures, neurodevelopmental impairment, and movement disorders. Ketogenic dietary therapies (KDT) are the gold standard treatment. Similar symptoms may appear in SLC2A1 negati...

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Detalles Bibliográficos
Autores principales: Ruiz Herrero, Jana, Cañedo Villarroya, Elvira, González Gutiérrez-Solana, Luis, García Alcolea, Beatriz, Gómez Fernández, Begoña, Puerta Macfarland, Laura Andrea, Pedrón-Giner, Consuelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000344/
https://www.ncbi.nlm.nih.gov/pubmed/33806661
http://dx.doi.org/10.3390/nu13030840

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000344/
https://www.ncbi.nlm.nih.gov/pubmed/33806661
http://dx.doi.org/10.3390/nu13030840

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