Results 11 to 20 of about 1,979 (168)

Eccentric Training as an Adjunct to Rehabilitation Program for Hereditary Multiple Exostoses: A Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Hereditary multiple exostoses an autosomal dominant skeletal disorder characterized by multiple cartilage-capped benign exostoses that typically occur in the metaphysis of long bones.
Zeynep Hazar Kanik   +4 more
doaj   +1 more source

Multiple Heriditary Exostoses in a Family for Three Generation of Indian Origin with Review of Literature [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2014
Multiple hereditary exostoses (MHE) are an autosomal dominant disorder, consisting of multiple cartilage capped bone tumour arising from the metaphysis of long tubular bones. Mutations are seen in Exostosin-1 and Exostosin-2 genes.
Kalyani R   +4 more
doaj   +1 more source

Minimally Invasive Total Hip Arthroplasty in a Patient with Hereditary Multiple Exostoses: A Case Report [PDF]

open access: yesMalaysian Orthopaedic Journal, 2018
Hip geometry abnormalities found in patients with hereditary multiple exostoses (HME) could promote premature hip joint degeneration which needs treatment.
Santoso A   +4 more
doaj   +1 more source

Hereditary multiple exostoses: A case report and literature review

open access: yesSAGE Open Medical Case Reports, 2022
Osteochondroma is the most common bone tumor representing 20%–50% of all benign bone tumors and 10%–15% of all bone tumors. Osteochondroma has similar radiological appearance in both solitary and multiple forms; the latter is an autosomal dominant ...
Thi Hien Ha   +6 more
doaj   +1 more source

Clinical and radiological characteristics of forearm deformities in children with multiple hereditary exostoses [PDF]

open access: yesГений oртопедии, 2019
Introduction The incidence of forearm deformities in children with multiple hereditary exostoses (MHE) ranges from 30 to 80 %. There are few studies of deformities of the forearm in MHE patients in the literature that describe not only the location of ...
Ekaterina A. Zakharyan   +2 more
doaj   +1 more source

Hereditary Multiple Exostoses with Ulnar Hemimelia

open access: yesProceedings, 2021
Hereditary Multiple Exostoses is a skeletal dysplasia that is very rare and defined by formation of numerous cartilage capped benign tumours either pedunculated or sessile known as osteochondromas throughout skeleton especially around the growth plates ...
Syed Wasif Ali Shah   +5 more
doaj   +1 more source

C2 intraspinal osteochondroma causing spinal cord compression in a patient with multiple hereditary exostoses

open access: yesIndian Spine Journal, 2022
Intraspinal osteochondroma causing neurological manifestations is a rare condition and can present as either solitary osteochondroma or more commonly as a part of multiple hereditary exostoses. We report a case of osteochondroma arising from lamina of C2
Janardhana P Aithala
doaj   +1 more source

Forearm deformities in children with hereditary multiple exostosis (review of literature) [PDF]

open access: yesГений oртопедии, 2020
Introduction Hereditary multiple exostoses, according to different authors, account for 16.0 to 43.0 % of all the cases of tumors, tumor-like and dysplastic diseases of the pediatric skeleton.
Alexander P. Pozdeev   +2 more
doaj   +1 more source

Spinal Exostosis in a Boy with Multiple Hereditary Exostoses

open access: yesCase Reports in Orthopedics, 2013
We report on a 13-year-old boy who presented with multiple hereditary exostosis and had development of back pain, associated with neurological deficits, and was found to have exostoses in the spinal canal.
Ali Al Kaissi   +3 more
doaj   +1 more source

Osteochondroma of rib cage in a case of HME: A rare presentation

open access: yesJournal of Orthopaedic Reports, 2023
Background: Osteochondroma is the most common benign bone tumor. This aberrant developmental lesion of the bone in the rib is rare and forms part of multiple diaphyseal aclasia in some cases.
Saroj prasad Sah   +5 more
doaj   +1 more source

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