Orofacial features and pediatric dentistry in the long-term management of Infantile Pompe Disease children

BACKGROUND: Glycogen storage disease type II (GSDII) or Pompe disease is a rare autosomal recessive metabolic disorder that leads to intracellular glycogen storage in many tissues, mainly in skeletal muscle, heart and liver. Facial muscle weakness and altered craniofacial growth are very common in P...

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Detalles Bibliográficos
Autores principales: Galeotti, Angela, De Rosa, Sara, Uomo, Roberto, Dionisi-Vici, Carlo, Deodato, Federica, Taurisano, Roberta, Olivieri, Giorgia, Festa, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685588/
https://www.ncbi.nlm.nih.gov/pubmed/33228748
http://dx.doi.org/10.1186/s13023-020-01615-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685588/
https://www.ncbi.nlm.nih.gov/pubmed/33228748
http://dx.doi.org/10.1186/s13023-020-01615-1

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