2-deoxy-2-[18]fluoro-D-glucose PET/CT (18FDG PET/CT) may not be a viable biomarker in Pompe disease

BACKGROUND: Pompe disease (PD) is an autosomal recessive, lysosomal storage disease due to a mutation of the acid α-glucosidase (GAA) gene. In adult patients, PD is characterized by slowly progressive limb-girdle and trunk myopathy and restrictive respiratory insufficiency. Enzyme replacement therap...

Descripción completa

Detalles Bibliográficos
Autores principales: Plöckinger, U., Prasad, V., Ziagaki, A., Tiling, N., Poellinger, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845361/
https://www.ncbi.nlm.nih.gov/pubmed/29523196
http://dx.doi.org/10.1186/s40246-018-0145-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5845361/
https://www.ncbi.nlm.nih.gov/pubmed/29523196
http://dx.doi.org/10.1186/s40246-018-0145-7

Ejemplares similares