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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...
Autores principales: | Yuldashev, Alisher J., Shin, Chang Ho, Kim, Yong Sung, Jang, Woo Young, Park, Moon Seok, Chae, Jong Hee, Yoo, Won Joon, Choi, In Ho, Kim, Ok Hwa, Cho, Tae-Joon |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Orthopaedic Association
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5334020/ https://www.ncbi.nlm.nih.gov/pubmed/28261436 http://dx.doi.org/10.4055/cios.2017.9.1.109 |
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