Results 11 to 20 of about 1,639 (208)

Hereditary multiple osteochondromas

open access: yesPortuguese Journal of Pediatrics
A three-year-old boy’s mother reports the appearance of painless swelling at the right tibia’s proximal end, with one year of evolution, without previous trauma or local/systemic inflammatory signs, namely fever or lymphadenopathy.
João R. Nunes-Pires   +2 more
doaj   +4 more sources

Hereditary multiple exostoses with a giant osteochondroma degenerated into chondrosarcoma

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   +4 more sources

Hereditary Multiple Exostoses—A Review of the Molecular Background, Diagnostics, and Potential Therapeutic Strategies

open access: yesFrontiers in Genetics, 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 ...
Ewelina Bukowska-Olech   +9 more
doaj   +3 more sources

Treatment of multiple hereditary osteochondromas of the forearm in children [PDF]

open access: yesThe Journal of Bone and Joint Surgery. British volume, 2006
We have evaluated the clinical outcomes of simple excision, ulnar lengthening and the Sauvé-Kapandji procedure in the treatment of deformities of the forearm in patients with multiple hereditary osteochondromas. The medical records of 29 patients (33 forearms) were reviewed; 22 patients (22 forearms) underwent simple excision (four with ulnar ...
E K, Shin, N F, Jones, J F, Lawrence
openaire   +4 more sources

Spinal cord stimulation for treatment of the pain associated with hereditary multiple osteochondromas. [PDF]

open access: yesJ Pain Res, 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
europepmc   +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

An extremely rare association of multiple familial trichoepitheliomas and hereditary multiple osteochondromas [PDF]

open access: yesInternational Journal of Dermatology, 2018
info:eu-repo/semantics ...
Monteiro, AF   +4 more
core   +3 more sources

Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas. [PDF]

open access: yesTurk Arch Pediatr, 2023
Hereditary multiple osteochondromas is an autosomal dominant disorder caused by heterozygous pathogenic variants in EXT1 or EXT2. We aimed to evaluate the clinical and molecular findings of a Turkish cohort with hereditary multiple osteochondroma.Thirty-two patients aged 1.3-49.6 years from 22 families were enrolled.
Güneş N   +9 more
europepmc   +4 more sources

Current concepts in the management of proximal femoral osteochondromas: a narrative review. [PDF]

open access: yesJ Orthop Surg Res
This narrative review synthesizes the latest advancements in the diagnosis and management of proximal femoral osteochondromas, underscoring the complexities of surgical intervention near neurovascular structures and the importance of precise imaging ...
Naghizadeh H   +3 more
europepmc   +2 more sources

A Family with Hereditary Multiple Exostoses [PDF]

open access: yesEurasian Journal of Family Medicine, 2021
Hereditary multiple exostoses is a rare autosomal dominant genetic disorder characterized by multiple exostoses (osteochondromas), mostly diagnosed in childhood.
Tahir Ismailoglu
doaj   +1 more source

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