Imaging findings of mucopolysaccharidoses: a pictorial review

INTRODUCTION: Mucopolysaccharidosis (MPS) represent a heterogeneous group of inheritable lysosomal storage diseases in which the accumulation of undegraded glycosaminoglycans (GAGs) leads to progressive damage of affected tissues. The typical symptoms include organomegaly, dysostosis multiplex, ment...

Descripción completa

Detalles Bibliográficos
Autores principales: Palmucci, Stefano, Attinà, Giancarlo, Lanza, Maria Letizia, Belfiore, Giuseppe, Cappello, Giuseppina, Foti, Pietro Valerio, Milone, Pietro, Di Bella, Domenico, Barone, Rita, Fiumara, Agata, Sorge, Giovanni, Ettorre, Giovanni Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Pictorial Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3731470/
https://www.ncbi.nlm.nih.gov/pubmed/23645566
http://dx.doi.org/10.1007/s13244-013-0246-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3731470/
https://www.ncbi.nlm.nih.gov/pubmed/23645566
http://dx.doi.org/10.1007/s13244-013-0246-8

Ejemplares similares