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AB042. Therapies for the bone in mucopolysaccharidoses
Patients with mucopolysaccharidoses (MPS) have accumulation of glycosaminoglycans in multiple tissues which may cause coarse facial features, mental retardation, recurrent ear and nose infections, inguinal and umbilical hernias, hepatosplenomegaly, and skeletal deformities. Clinical features related...
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| 發表在: | Ann Transl Med |
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| 主要作者: | |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
AME Publishing Company
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4563430/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB042 |
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