Case Report: The Association of Wilson Disease in a Patient With Ataxia and GLUT-1 Deficiency

Background: Wilson disease (WD) and glucose transporter type 1 (GLUT1) deficiency syndrome are two syndromes with different modes of inheritance but share certain similarities on neurological presentation. To date we have not found previous reports of an association between these two disorders. Case...

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Detalles Bibliográficos
Autores principales: Diaz, Jenna, Fonseca, Ashley G., Arboleda, Richard, Frade, Alejandro, Gennaro, Maria Pilar, Jayakar, Parul, Schleifer, Paula, Hernandez, Erick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524673/
https://www.ncbi.nlm.nih.gov/pubmed/34676189
http://dx.doi.org/10.3389/fped.2021.750593

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8524673/
https://www.ncbi.nlm.nih.gov/pubmed/34676189
http://dx.doi.org/10.3389/fped.2021.750593

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