Results 11 to 20 of about 1,261 (184)

Hereditary multiple exostoses with a giant osteochondroma degenerated into chondrosarcoma [PDF]

open access: yesRadiology Case Reports
We present a case of hereditary multiple exostoses with malignant transformation to chondrosarcoma in a woman complaining of enlargement and pain in the right thigh.
Federica Masino, MD   +6 more
doaj   +5 more sources

An Abnormal Presentation of a Popliteal Artery Mass and a Unique Cause of Claudication [PDF]

open access: yesCase Reports in Orthopedics
Multiple hereditary exostosis (MHE) is a rare autosomal-dominant disorder marked by multiple osteochondromas arising from the metaphyses of long bones.
Jamil Haddad   +4 more
doaj   +3 more sources

Current paediatric orthopaedic practice in hereditary multiple osteochondromas of the forearm: a systematic review [PDF]

open access: yesSICOT-J, 2018
Introduction: This systematic review aims to answer three research questions concerning the management of hereditary multiple osteochondromas of forearm in children: What is the best available evidence for the currently employed surgical procedures? What
EL-Sobky Tamer A.   +5 more
doaj   +4 more sources

Two Siblings Followed Up for Hereditary Multiple Exostoses [PDF]

open access: yesHaseki Tıp Bülteni, 2014
Hereditary multiple exostoses is an autosomal dominant disease with abnormal bone formation especially at the long bones. Osteochondromas, which occur in the course of the disease, can cause growth disturbances in affected children.
Meltem Erol   +7 more
doaj   +2 more sources

Bone deformities with hereditary multiple osteochondromas [PDF]

open access: yesDanish Medical Journal
INTRODUCTION. Hereditary multiple osteochondromas (HMO) is a genetic skeletal disorder caused by defects in exostosin glycosyltransferase 1 (EXT1) or 2 (EXT2) genes. It develops mainly in the growth period and causes multiple osteochondromas (OC) in the physis of the long bones, leading to discomfort and deformities. This study aimed to investigate the
Brink Petersen, Rikke   +3 more
openaire   +5 more sources

Bilateral scapulothoracic osteochondromas in a patient with hereditary multiple exostosis: a case report and review of the literature [PDF]

open access: yesOrthopedic Reviews, 2016
Hereditary multiple exostosis (HME) is an autosomal dominant disorder characterized by two or more benign growing, cartilage capped tumors of long bones called osteochondromas.
Markus Rupp   +3 more
doaj   +3 more sources

A 40-Year-Old Male Presenting with Hereditary Multiple Exostosis: Management and Considerations [PDF]

open access: yesCase Reports in Orthopedics, 2019
Hereditary multiple exostosis is a rare condition in which numerous benign osteochondromas form throughout the body, typically in areas of high bone turnover such as the metaphyseal plates of long bones.
Matthew Wells, Zackary Birchard
doaj   +2 more sources

Osteochondroma Arising from Dorsal Pedicle Causing Compressive Myelopathy [PDF]

open access: yesJournal of Orthopaedic Case Reports
Introduction: Osteochondromas are benign bony neoplasms typically located in long bones, though they may occasionally occur in the posterior elements of the spine.
Mantu Jain   +5 more
doaj   +2 more sources

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

Prevalence of Osteochondromas in the Spine in Patients with Multiple Hereditary Exostoses

open access: yesJBJS Open Access
Background:. Multiple hereditary exostoses (MHE) is an autosomal-dominant disorder characterized by the development of multiple cartilage-capped exostoses originating from the physis that are known as osteochondromas.
Carlos Monroig-Rivera, MD   +4 more
doaj   +3 more sources

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