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...

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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

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