Results 21 to 30 of about 288 (135)

An Unusual Presentation of Chondrosarcoma in Diaphyseal Aclasis

open access: yesInternational Journal of Clinical Practice, 1982
H, Deshpande, M K, Browne
openaire   +4 more sources

Imaging of Pediatric Benign Bone Tumors [PDF]

open access: yes, 2021
Benign bone tumors in the pediatric population can have varied clinical presentations ranging from asymptomatic to nonspecific pain, swelling, or pathological fracture.
Chauhan, Ankita, Shah, Jignesh
core   +2 more sources

Hereditary Multiple Osteochondroma with Incomplete Penetrance in a Lebanese Family: A Case Report [PDF]

open access: yes, 2021
Background: Hereditary multiple osteochondroma (HMO) is a rare autosomal dominant disease with high penetrance reaching 95 to 100%. It manifests during childhood in most of the times. The spectrum of the disease is wide.
Alayane, Ali   +7 more
core   +1 more source

Biology of bone sarcomas and new therapeutic developments [PDF]

open access: yes, 2017
Bone sarcomas are tumours belonging to the family of mesenchymal tumours and constitute a highly heterogeneous tumour group. The three main bone sarcomas are osteosarcoma, Ewing sarcoma and chondrosarcoma each subdivided in diverse histological entities.
Brown, H.K.   +4 more
core   +1 more source

Leg fracture associated with synostosis of interosseous membrane during running in a soccer player [PDF]

open access: yes, 2017
ntroduction - Leg fractures may occur frequently in sport injuries but it is very rare to find this kind of injury associated with interosseous membrane synostosis.
Buharaja, Rodrigo   +3 more
core   +1 more source

The role of arthrography in the management of dysplasia epiphysealis hemimelica [PDF]

open access: yes, 1986
Dysplasia epiphysealis hemimelica can be diagnesed on plain radiographs of the affected areas. However, double contrast arthrography in three new cases provided additional information.
Blane, Caroline E.   +2 more
core   +1 more source

Gradual Lengthening of the Ulna in Patients with Multiple Hereditary Exostoses with a Dislocated Radial Head [PDF]

open access: yes, 2014
PURPOSE: Multiple hereditary exostoses of the forearm typically form in the distal ulna, causing disturbances in the growth of the ulna and functional disability.
조영진
core   +1 more source

Gradual ulnar lengthening in children with multiple exostoses and radial head dislocation: results at skeletal maturity [PDF]

open access: yes, 2016
Purpose: Deformities of the forearm and shortening of the ulna occur in 30 % of patients with hereditary multiple exostoses (HME), leading to radial head dislocation and loss of movement. Several surgical techniques have been described for treatment,
Barbato A.   +4 more
core   +1 more source

Diaphyseal aclasis affecting the temporomandibular joint

open access: yesDentomaxillofacial Radiology, 1999
Abstract Diaphyseal aclasis is a rare disorder of bone development in which multiple, cartilagenous exostoses develop and enlarge mainly on the ends of long bones. It has also been described in the vertebral column where it may give rise to spinal cord compression but has not previously been reported as occurring in the jaws.
G A, Welsh, I, MacLeod
openaire   +2 more sources

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