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Orthopedic Manifestations of Type I Camurati-Engelmann Disease
BACKGROUND: Camurati-Engelmann disease (CED) is a rare genetic skeletal disorder characterized by limb pain, muscle emaciation and weakness, and cortical thickening of the diaphysis of long bones. It is caused by mutations in the transforming growth factor beta 1 (TGFB1) (type I) or other unknown ge...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Clin Orthop Surg |
|---|---|
| Prif Awduron: | , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
The Korean Orthopaedic Association
2017
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5334020/ https://ncbi.nlm.nih.gov/pubmed/28261436 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4055/cios.2017.9.1.109 |
| Tagiau: |
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