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Bilateral Symmetrical Cortical Osteolytic Lesions in Two Patients with Gaucher Disease
Gaucher disease (GD) is an autosomal recessive lysosomal storage disorder characterized by the reduced or absent activity of glucocerebrosidase. The disease is split into three types. Type 3, or chronic neuronopathic GD, manifests with heterogeneous clinical presentations. Skeletal manifestations of...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3348707/ https://ncbi.nlm.nih.gov/pubmed/21935720 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00256-011-1260-x |
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