Cardiac disease in children and young adults with various lysosomal storage diseases: Comparison of echocardiographic and ECG changes among clinical groups

BACKGROUND: Lysosomal storage disease (LSD) is a rare inherited disease group. Consecutively there are few data on cardiac changes in mucopolysaccharidosis (MPS), Anderson Fabry disease (AFD), and other LSD (oLSD) including Pompe disease (PD) and Danon disease (DD), I-cell disease ICD and mucolipido...

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Detalles Bibliográficos
Autores principales: Mueller, P., Attenhofer Jost, C.H., Rohrbach, M., Valsangiacomo Buechel, E.R., Seifert, B., Balmer, C., Kretschmar, O., Baumgartner, M.R., Weber, R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801096/
https://www.ncbi.nlm.nih.gov/pubmed/29450157
http://dx.doi.org/10.1016/j.ijchv.2013.10.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801096/
https://www.ncbi.nlm.nih.gov/pubmed/29450157
http://dx.doi.org/10.1016/j.ijchv.2013.10.002

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