Results 1 to 10 of about 713 (172)

Hereditary multiple exostoses (HME) [PDF]

open access: yesAtlas of Genetics and Cytogenetics in Oncology and Haematology, 2011
Review on Hereditary multiple exostoses (HME), with data on clinics, and the genes involved.
Bovée, JVMG
openaire   +4 more sources

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   +3 more sources

Hereditary Multiple Exostoses with Rare Ocular Finding: A Case Report [PDF]

open access: yesJournal of Current Ophthalmology, 2023
Purpose: To study rare ocular findings in a rare case of hereditary multiple exostoses (HME) and to study HME in one family. Methods: HME is an autosomal dominant genetic disease characterized by the presence of multiple exostoses (osteochondromas).
Shashi Tanwar   +3 more
doaj   +2 more sources

Management of Lower Extremity Deformity in Children with Hereditary Multiple Exostoses [PDF]

open access: yesJournal of the Pediatric Orthopaedic Society of North America
Hereditary multiple exostoses (HME) is a rare genetic disorder characterized by multiple benign, cartilage-capped bony tumors, most often found at the juxta-epiphyseal regions of long bones.
Matthew J. Whalen, MS   +1 more
doaj   +2 more sources

Hereditary multiple exostoses and porencephaly in a Nigerian child: a case report [PDF]

open access: yesThe Pan African Medical Journal, 2018
Hereditary multiple exostoses (HME) is a rare condition that is characterised by the outgrowth of bony swellings, usually from the growth ends of long bones. It is autosomal dominant, and may result in debilitating deformities.
Idris Abiodun Adedeji   +4 more
doaj   +3 more sources

An unusual example of hereditary multiple exostoses: a case report and review of the literature [PDF]

open access: yesBMC Musculoskeletal Disorders, 2021
Background Hereditary multiple exostoses (HME) is a rare skeletal disorder characterised by a widespread. distribution of osteochondromas originating from the metaphyses of long bones. Case presentation This case study examines a 55-year-old male cadaver
Rebecca Chilvers   +3 more
doaj   +2 more sources

Cervical Myelopathy Caused by Disc Herniation at the Segment of Existing Osteochondroma in a Patient with Hereditary Multiple Exostoses [PDF]

open access: yesAsian 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
doaj   +4 more sources

Costal chondrosarcoma in a woman with hereditary multiple exostoses - a case report [PDF]

open access: yesFrontiers in Oncology
In this report, we present a case of a 32-year-old female previously diagnosed with hereditary multiple exostoses(HME) who was incidentally found to have an asymptomatic anterior mediastinal mass during a routine examination.
Ze Yang, Kaiqiang Wang, Jiangtao Pu
doaj   +2 more sources

Hereditary Multiple Exostoses: Clinical, Molecular and Radiologic Survey in 9 Families [PDF]

open access: yesPrague Medical Report, 2017
Hereditary multiple exostoses (HME) represents a heterogeneous group of diseases often associated with progressive skeletal deformities. Most frequently, mutations in EXT1 and EXT2 genes with autosomal dominant inheritance are responsible for HME. In our
Karel Medek   +9 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

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