Results 11 to 20 of about 20,986 (228)

Hereditary Multiple Exostoses-A Review of the Molecular Background, Diagnostics, and Potential Therapeutic Strategies. [PDF]

open access: yesFront Genet, 2021
Hereditary multiple exostoses (HMEs) syndrome, also known as multiple osteochondromas, represents a rare and severe human skeletal disorder. The disease is characterized by multiple benign cartilage-capped bony outgrowths, termed exostoses or ...
Bukowska-Olech E   +8 more
europepmc   +2 more sources

Spontaneous Regression of Multiple Osteochondromas in a Patient With Hereditary Multiple Exostoses: A Case Report. [PDF]

open access: yesCureus
Hereditary multiple exostoses (HME) is an autosomal dominant disorder characterized by the development of multiple osteochondromas, primarily near the metaphyses of long bones.
Ikeda K, Teruya S, Tsuge H, Onishi S.
europepmc   +2 more sources

Ulnar lengthening in the treatment of forearm deformity caused by hereditary multiple exostoses in children. [PDF]

open access: yesWorld J Orthop
Hereditary multiple exostoses (HME) is an autosomal dominant bone disorder characterized by abnormal bone development. HME mostly involves the forearm, resulting in forearm deformities, limited functional activities, etc.
Wang S   +7 more
europepmc   +2 more sources

A Rare Case of Hereditary Multiple Exostoses in a Woman. [PDF]

open access: yesOrthop Nurs
Hereditary multiple exostosis (HME) is a rare genetic disorder characterized by multiple bony spurs or lumps, commonly affecting the long bones. This case report exposes the clinical presentation, diagnosis, and management of HME in a 28-year-old female ...
Ghamri RA.
europepmc   +2 more sources

Intrathecal Fentanyl Pump Placement in a Patient With Chronic Pain Caused by Hereditary Multiple Exostoses: A Case Report. [PDF]

open access: yesCureus
Hereditary multiple exostoses (HME) is a genetic disorder defined by the formation of benign bone tumors known as exostoses, which can lead to chronic pain and functional impairment. This case report details a 57-year-old man with a long-standing history
Tageant H   +5 more
europepmc   +2 more sources

Haploinsufficiency of EXT1 and Heparan Sulphate Deficiency Associated with Hereditary Multiple Exostoses in a Pakistani Family. [PDF]

open access: yesMedicina (Kaunas), 2022
Background and Objectives: Hereditary multiple exostoses (HME) is a disease characterized by cartilage-capped bony protuberances at the site of growth plates of long bones.
Ajmal M   +5 more
europepmc   +2 more sources

An Unusual Presentation of Costal Intraspinal Osteochondroma Causing Compressive Myelopathy in a Patient With Hereditary Multiple Exostoses: A Case Report and Literature Review. [PDF]

open access: yesCureus
A 22-year-old man presented to us with back pain for four months, inability to walk, and weakness in both lower limbs. Clinical examination revealed multiple swellings in the body, motor weakness, paresthesia, and upper motor neuron signs.
Jeevo J, N V A, Shekoba M.
europepmc   +2 more sources

Ulnar lengthening for children with forearm deformity from hereditary multiple exostoses: a retrospective study from a tertiary medical center. [PDF]

open access: yesBMC Pediatr
Patients with hereditary multiple exostosis (HME) usually present with forearm deformity with or without radial head dislocation. Ulna lengthening has been proposed to address this condition.
Wang S   +6 more
europepmc   +2 more sources

Osteochondroma formation is independent of heparanase expression as revealed in a mouse model of hereditary multiple exostoses. [PDF]

open access: yesJ Orthop Res, 2022
Hereditary multiple exostoses (HME) is a rare, pediatric disorder characterized by osteochondromas that form along growth plates and provoke significant musculoskeletal problems.
Mundy C   +5 more
europepmc   +2 more sources

Clinical survey of a pedigree with hereditary multiple exostoses and identification of EXT‑2 gene deletion mutation. [PDF]

open access: yesMol Med Rep, 2022
The aim of the present study was to report a clinical survey of hereditary multiple exostoses (HME) in a large Chinese pedigree, and the identification of a novel deletion mutation of exostosin glycosyltransferase 2 (EXT-2) gene.
Wang W   +8 more
europepmc   +2 more sources

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