Identification of a rare case of intra-articular osteochondroma manifesting as three loose bodies in a patient with hereditary multiple osteochondromas: A case report

Hereditary multiple osteochondromas (HMO) is an autosomal dominant bone disorder characterised by the presence of multiple benign cartilage-capped tumours. Exostosin-1 (EXT1) and EXT2 are the major morbigenous genes associated with HMO, mutations in which are responsible for 90% of all HMO cases. In...

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Veröffentlicht in:Oncol Lett
Hauptverfasser: KONG, MINGXIANG, CAO, LI, ZHANG, QIONG, FANG, YONG, ZHAO, CHEN, GU, HAIFENG, ZHANG, SHUIJUN, CHEN, YU, WU, JINHUA, BI, QING
Format: Artigo
Sprache:Inglês
Veröffentlicht: D.A. Spandidos 2015
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Articles
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4509409/
https://ncbi.nlm.nih.gov/pubmed/26622573
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/ol.2015.3284
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