Nutritional management of glycogen storage disease type III: a case report and a critical appraisal of the literature

Glycogen storage disease Type III (GSD III) is an autosomal recessive disease due to the deficiency of the debranching enzyme, which has two main consequences: a reduced availability of glucose due to the incomplete degradation of glycogen, and the accumulation of abnormal glycogen in liver and card...

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Detalles Bibliográficos
Autores principales: Massimino, Elena, Amoroso, Anna Paola, Lupoli, Roberta, Rossi, Alessandro, Capaldo, Brunella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Nutrition
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213733/
https://www.ncbi.nlm.nih.gov/pubmed/37252245
http://dx.doi.org/10.3389/fnut.2023.1178348

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213733/
https://www.ncbi.nlm.nih.gov/pubmed/37252245
http://dx.doi.org/10.3389/fnut.2023.1178348

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