Impact on bone microarchitecture and failure load in a patient with type I Gaucher disease who switched from Imiglucerase to Eliglustat

Gaucher disease (GD; OMIM 230800) is a lysosomal storage disorder caused by a deficiency in acid beta-glucosidase as a result of mutation in the GBA gene. Type 1 GD (GD1) is the most common form and its clinical manifestations include severe hematological, visceral and bone disease. The goal of dise...

Descripción completa

Detalles Bibliográficos
Autores principales: Sidhu, Karamjot, Boyd, Steven K., Khan, Aneal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264072/
https://www.ncbi.nlm.nih.gov/pubmed/32509532
http://dx.doi.org/10.1016/j.ymgmr.2020.100606

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264072/
https://www.ncbi.nlm.nih.gov/pubmed/32509532
http://dx.doi.org/10.1016/j.ymgmr.2020.100606

Ejemplares similares