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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Bibliographic Details
Published in:Clin Orthop Surg
Main Authors: 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
Format: Artigo
Language:Inglês
Published: The Korean Orthopaedic Association 2017
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Original Article
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
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