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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Clin Orthop Surg
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The Korean Orthopaedic Association 2017
Pynciau:
Original Article
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
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