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Osteopenia in Gaucher disease develops early in life: Response to imiglucerase enzyme therapy in children, adolescents and adults

BACKGROUND: In Gaucher disease (GD), acid-β-glucosidase (GBA1) gene mutations result in defective glucocerebrosidase and variable combinations of hematological, visceral, and diverse bone disease. Osteopenia is highly prevalent, but its age of onset during the natural course of GD is not known. It i...

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Autors principals: Mistry, Pramod K., Weinreb, Neal J., Kaplan, Paige, Cole, J. Alexander, Gwosdow, Andrea R., Hangartner, Thomas
Format: Artigo
Idioma:Inglês
Publicat: 2010
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3019260/
https://ncbi.nlm.nih.gov/pubmed/21112800
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bcmd.2010.10.011
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