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

open access: yesTurk Arch Pediatr, 2023
Objective: 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 ...
Güneş N   +9 more
europepmc   +2 more sources

Rare retro-patellar multiple osteochondromas in patellar tendon: A case report. [PDF]

open access: yesClin Case Rep, 2023
Osteochondromas (OCs) are developmental anomalies that originate from the periosteum and typically form during enchondral ossification near the joints. Retro‐patellar OC caused by exostosis forms in various intracapsular, intra‐tendon, and joint‐adjacent
Pirmohamadi H   +3 more
europepmc   +2 more sources

Chondrosarcoma secondary to hereditary multiple osteochondromas with spinal cord compression: A case report and systematic review. [PDF]

open access: yesSurg Neurol Int, 2023
Background: Hereditary multiple osteochondromas (HMOs) are a rare genetic disorder characterized by the formation of multiple benign osteochondromas that can undergo malignant transformation into chondrosarcoma.
Silva JE   +7 more
europepmc   +2 more sources

Modified gradual ulnar lengthening for treatment of Masada type IIb forearm deformity in children with hereditary multiple osteochondromas. [PDF]

open access: yesFront Pediatr, 2023
Objective To investigate the effect of modified gradual ulnar lengthening in the treatment of Masada type IIb forearm deformity in children with hereditary multiple osteochondromas (HMO).
Fan J   +5 more
europepmc   +2 more sources

Paediatric Calcaneal Osteochondroma: A Case Report and a Literature Review [PDF]

open access: yesDiseases
Background: Heel pain in children is a common condition. The aetiology can be ascribed to fractures, osteochondrosis, tendinitis, calcaneal-navicular or talo-calcaneal coalition, osteomyelitis, rheumatic diseases, anatomic variants, malignant tumours ...
Valeria Calogero   +5 more
doaj   +3 more sources

Arthroscopic Anterior Cruciate Ligament Reconstruction in a 17-Year-Old Female Athlete with Multiple Hereditary Exostoses Using a Peroneus Longus Autograft: A Rare Case Report [PDF]

open access: yesJournal of Orthopaedic Case Reports
Introduction: Hereditary multiple exostoses, also known as multiple osteochondromas, is a rare genetic disorder marked by the formation of osteocartilaginous outgrowths predominantly near the metaphysis of long bones.
Sanjay Singh Chauhan   +2 more
doaj   +2 more sources

Pain and fatigue in adult patients with multiple osteochondromas: The Netherlands. [PDF]

open access: yesPLoS One
Background Multiple Osteochondromas (MO) is a rare genetic disorder characterised by the presence of numerous benign bone tumours, known as osteochondromas.
Amajjar I   +4 more
europepmc   +2 more sources

Millennium-old pathogenic Mendelian mutation discovery for multiple osteochondromas from a Gaelic Medieval graveyard. [PDF]

open access: yesEur J Hum Genet, 2023
Only a limited number of genetic diseases are diagnosable in archaeological individuals and none have had causal mutations identified in genome-wide screens. Two individuals from the Gaelic Irish Medieval burial ground of Ballyhanna, Co.
Jackson I   +4 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

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