Bone density in patients with late onset Pompe disease

BACKGROUND: Pompe disease is an inherited metabolic disorder characterized by α-glycosidase deficiency, which leads to lysosomal glycogen accumulation in many different tissues. The infantile form is the most severe with a rapidly fatal outcome, while the late onset form has a greater phenotypic var...

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Detalles Bibliográficos
Autores principales: Papadimas, George, Terzis, Gerassimos, Papadopoulos, Constantinos, Areovimata, Anna, Spengos, Konstantinos, Kavouras, Stavros, Manta, Panagiota
Formato: Artigo
Lenguaje:Inglês
Publicado: Kowsar 2012
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Original Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3693639/
https://ncbi.nlm.nih.gov/pubmed/23843830
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5812/ijem.4967
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