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...

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Detalles Bibliográficos
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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Orthopaedic Association 2017
Materias:
Original Article
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

Internet

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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