Results 11 to 20 of about 1,923 (159)

Malignancy Ratio in Pediatric Patients with Hereditary Multiple Exostoses: True Association or Reporting Bias? [PDF]

open access: yesPediatric Reports
Background: Hereditary Multiple Exostoses (HME) is a rare autosomal dominant skeletal disorder resulting from loss-of-function variants in the EXT1, EXT2, or EXT3 genes. While malignant transformation into chondrosarcoma is well documented, the incidence
Francesco Fabrizio Comisi   +3 more
doaj   +2 more sources

Hereditary multiple exostoses

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Hasan Ekim, Meral Ekim
doaj   +3 more sources

Spinal stenosis frequent in children with multiple hereditary exostoses [PDF]

open access: yesJournal of Children's Orthopaedics, 2013
Purpose Children with multiple hereditary exostoses (MHE) have numerous osteochondromas, with the most prominent lesions typically over the appendicular skeleton.
Ali Ashraf   +5 more
doaj   +2 more sources

A Family with Hereditary Multiple Exostoses [PDF]

open access: yesEurasian Journal of Family Medicine, 2021
Hereditary multiple exostoses is a rare autosomal dominant genetic disorder characterized by multiple exostoses (osteochondromas), mostly diagnosed in childhood.
Tahir Ismailoglu
doaj   +1 more source

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

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

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

Home - About - Disclaimer - Privacy