Current paediatric orthopaedic practice in hereditary multiple osteochondromas of the forearm: a systematic review [PDF]
SICOT-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
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Bone deformities with hereditary multiple osteochondromas [PDF]
Danish Medical JournalINTRODUCTION. 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
Ruth Petersen +3 more
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Hereditary multiple osteochondromas in a child: a case report and discussion of postoperative complication management [PDF]
Frontiers in SurgeryBackgroundThe pathogenesis of hereditary multiple exostoses is mainly related to genetic variants and often requires surgical resection when it causes clinical symptoms.
Haiting Jia, Yuting Wang, Tao Liu
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Hereditary multiple osteochondromas in Jordanian patients: Mutational and immunohistochemical analysis of EXT1 and EXT2 genes. [PDF]
Oncol Lett, 2021 Mohaidat Z +6 more
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Modified gradual ulnar lengthening for treatment of Masada type IIb forearm deformity in children with hereditary multiple osteochondromas. [PDF]
Front Pediatr, 2023 Fan J +5 more
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Cervical Myelopathy Caused by Disc Herniation at the Segment of Existing Osteochondroma in a Patient with Hereditary Multiple Exostoses [PDF]
Asian Spine Journal, 2014 Hereditary multiple exostoses (HME) is a benign hereditary disorder characterized by multiple osteochondromas. Osteochondroma appears occasionally in the spinal column as a part of HME.
Ko Ikuta +5 more
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Spinal cord stimulation for treatment of the pain associated with hereditary multiple osteochondromas [PDF]
Journal of Pain Research, 2015 Ravi G Mirpuri,1 Jereme Brammeier,2 Hamilton Chen,2 Frank PK Hsu,1,3 Vi K Chiu,4 Eric Y Chang1,2,5 1Department of Physical Medicine and Rehabilitaiton, 2Department of Anesthesiology and Perioperative Care, 3Department of Neurological Surgery, 4Department
Mirpuri RG +5 more
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Genetic screening of EXT1 and EXT2 in Cypriot families with hereditary multiple osteochondromas
Journal of Genetics, 2015 The purpose of this study was to perform genetic screening of the exostosin 1 (EXT1) and exostosin 2 (EXT2) genes in Cypriot patients with a clinical diagnosis of hereditary multiple osteochondromas (HMO). Initially, mutation analysis of the EXT1 gene was performed by Sanger sequencing.
George A. Tanteles +10 more
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A special type hereditary multiple osteochondroma in patients with proximal ulna osteochondroma [PDF]
Abstract Background: Hereditary Multiple Osteochondroma (HMO) is a rare condition that frequently impacts the forearm and results in radial head dislocation. Consequently, orthopedic surgeons prioritize prognostication of factors contributing to radial head dislocation and implementing preventive measures.
Yan An +8 more
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HSPG-deficient zebrafish uncovers dental aspect of multiple osteochondromas. [PDF]
PLoS ONE, 2012 Multiple Osteochondromas (MO; previously known as multiple hereditary exostosis) is an autosomal dominant genetic condition that is characterized by the formation of cartilaginous bone tumours (osteochondromas) at multiple sites in the skeleton ...
Malgorzata I Wiweger +4 more
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