Loading...
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...
Saved in:
| Published in: | Clin Orthop Surg |
|---|---|
| Main Authors: | , , , , , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
The Korean Orthopaedic Association
2017
|
| Subjects: | |
| Online Access: | 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 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|