Case report: Chronic pain in a pediatric patient with late-onset pompe disease

Pompe disease (PD) is a rare inherited metabolic disorder of deficient or absent acid alpha-glucosidase (GAA), resulting in defective lysosomal glycogen catabolism. Muscle weakness, respiratory deficiency and gastrointestinal symptoms are commonly monitored in PD. However, pain and associated psycho...

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Detalles Bibliográficos
Autores principales: Cao, Amanda, van Gool, Raquel, Golden, Emma, Goodlett, Benjamin, Camelo, Carlos, Bujoreanu, Simona, Al-Hertani, Walla, Upadhyay, Jaymin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pain Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10575478/
https://www.ncbi.nlm.nih.gov/pubmed/37841659
http://dx.doi.org/10.3389/fpain.2023.1244609

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10575478/
https://www.ncbi.nlm.nih.gov/pubmed/37841659
http://dx.doi.org/10.3389/fpain.2023.1244609

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