Results 21 to 30 of about 4,012 (251)

Genotype-phenotype correlation in hereditary multiple exostoses [PDF]

open access: bronze, 2001
Hereditary multiple exostoses (EXT; MIM 133700) is an autosomal dominant bone disorder characterized by the presence of multiple benign cartilage-capped tumors (exostoses).
Christine Francannet
openalex   +3 more sources

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   +5 more sources

Longitudinal Observation of Changes in the Ankle Alignment and Tibiofibular Relationships in Hereditary Multiple Exostoses [PDF]

open access: yesDiagnostics, 2020
The longitudinal changes in the tibiofibular relationship as the ankle valgus deformity progresses in patients with hereditary multiple exostoses (HME) are not well-known.
Jae Hoo Lee   +5 more
doaj   +2 more sources

C1 C2 spinal cord compression in hereditary multiple exostoses: case report and review of the literature [PDF]

open access: goldInt J Surg Case Rep, 2021
Nesrine Jemel   +4 more
openalex   +2 more sources

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

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

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