Early diagnosis and management of cardiac manifestations in mucopolysaccharidoses: a practical guide for paediatric and adult cardiologists

Mucopolysaccharidoses (MPS) are a group of hereditary disorders caused by lysosomal storage of glycosaminoglycans (GAGs) and characterized by a wide variability of phenotypes from severe fetal-neonatal forms to attenuated diseases diagnosed in adult individuals. The clinical picture generally worsen...

Descripción completa

Detalles Bibliográficos
Autores principales: Boffi, Lucia, Russo, Pierluigi, Limongelli, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238246/
https://www.ncbi.nlm.nih.gov/pubmed/30442163
http://dx.doi.org/10.1186/s13052-018-0560-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238246/
https://www.ncbi.nlm.nih.gov/pubmed/30442163
http://dx.doi.org/10.1186/s13052-018-0560-3

Ejemplares similares