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Coxarthritis as the Presenting Symptom of Gaucher Disease Type 1
Gaucher disease (GD) type 1 is the most common lysosomal storage disorder due to beta glucocerebrosidase deficiency leading to an abnormal accumulation of its substrate, glucocerebroside, in the mononuclear phagocyte system. The disease presentation is usually characterized by signs and symptoms rel...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3199935/ https://ncbi.nlm.nih.gov/pubmed/22046515 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2011/361279 |
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