Multiple osteochondromas (MO) is characterised by development of two or more cartilage capped bony outgrowths (osteochondromas) of the long bones. The prevalence is estimated …
This WHO classification covers tumors of soft tissue and bone including inherited tumor syndromes. Each entity is extensively discussed with information on clinicopathological …
With complete coverage appropriate for residents through experienced pediatric orthopaedic surgeons, Tachdjian's Pediatric Orthopaedics, 6th Edition, continues a 50-year …
The classic text on the Mayo Clinic's experience with bone tumors is now in its updated Sixth Edition. Dahlin's Bone Tumors presents a succinct, profusely illustrated summary of the …
GA Schmale, EU Conrad 3rd, WH Raskind - Jbjs, 1994 - journals.lww.com
We established a database of hereditary multiple exostoses for the state of Washington, on the basis of a retrospective review of the medical records and a clinical evaluation of family …
P Kitsoulis, V Galani, K Stefanaki, G Paraskevas… - In vivo, 2008 - iv.iiarjournals.org
Osteochondroma is the most common benign bone tumor and usually occurs in the metaphyseal region of the long bones. This tumor takes the form of a cartilage-capped bony …
CL Wicklund, RM Pauli, D Johnston… - American journal of …, 1995 - Wiley Online Library
Hereditary multiple exostosis (EXT) is an autosomal dominant disorder in which the clinical hallmark is the growth of bony protuberances from long bones and which can cause a …
RC Hennekam - Journal of medical genetics, 1991 - ncbi.nlm.nih.gov
Exostoses that affect" almost every bone in the body" were first mentioned by John Hunter in his Lectures on the principles of surgery in 1786.1 The first family affected by HME was …
W Wuyts, W Van Hul - Human mutation, 2000 - Wiley Online Library
Hereditary multiple exostoses (EXT) is an autosomal dominant disorder characterized by the formation of exostoses, which are cartilage‐capped bony protuberances mainly located on …