Results 1 to 10 of about 9,014 (240)

Outcomes of Temporary Hemiepiphyseal Stapling for Correcting Genu Valgum in Children with Multiple Osteochondromas: A Single Institution Study

open access: yesChildren, 2021
Background: Multiple osteochondromas is a rare skeletal disorder characterized by the presence of osteocartilaginous protrusions causing bony deformities, especially around the knee.
Giovanni Trisolino   +2 more
exaly   +4 more sources

Multiple osteochondromas [PDF]

open access: yesOrphanet Journal of Rare Diseases, 2008
Multiple osteochondromas (MO) is characterised by development of two or more cartilage capped bony outgrowths (osteochondromas) of the long bones. The prevalence is estimated at 1:50,000, and it seems to be higher in males (male-to-female ratio 1.5:1 ...
Judith V M G Bovée
exaly   +5 more sources

Multiple osteochondromas of the antlers and cranium in a free-ranging white-tailed deer (Odocoileus virginianus). [PDF]

open access: yesPLoS ONE, 2017
This paper reports a case of multiple osteochondromas affecting the antlers and the left zygomatic bone of a free-ranging adult white-tailed buck (Odocoileus virginianus) from Georgia, USA.
Uwe Kierdorf   +4 more
doaj   +8 more sources

The Rizzoli Multiple Osteochondromas Classification revised: describing the phenotype to improve clinical practice

open access: yesAmerican Journal of Medical Genetics, Part A, 2021
Multiple osteochondromas (MO) is a rare disorder, characterized by benign osteocartilaginous tumors (osteochondromas), arising from the perichondrium of bones.
Marina Mordenti   +2 more
exaly   +2 more sources

The natural history of multiple osteochondromas in a large Italian cohort of pediatric patients

open access: yesBone, 2020
IMPORTANCE Multiple osteochondromas is a rare hereditary skeletal disorder, characterized by bony protrusions arising from growth plates on long bones during skeletal development.
Marina Mordenti   +2 more
exaly   +2 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

Differentiation of Pediatric Osteochondroma From Trevor's Disease and Successful Surgical Management: A Case Report. [PDF]

open access: yesCase Rep Orthop
Osteochondroma is the most common benign bone tumor; however, its presentation in the small bones of the appendicular skeleton, particularly the talus and subtalar joint, is quite rare. Although most cases of osteochondroma are asymptomatic, symptomatic presentations can lead to joint deformity, pain, swelling, tarsal tunnel syndrome, gait alterations,
Montalbano A   +3 more
europepmc   +2 more sources

Dysplasia epiphysealis hemimelica: A histological comparative study with osteochondromas

open access: yesJournal of Children's Orthopaedics, 2017
Purpose Dysplasia epiphysealis hemimelica (DEH) is a rare developmental disorder resulting in epiphyseal overgrowth. Based on histological appearance, it is often described as an osteochondroma or osteochondroma-like lesion, although clinical differences
J. Stevens   +4 more
doaj   +2 more sources

Osteochondromas of the cervical spine-case series and review

open access: yesJournal of Clinical Orthopaedics and Trauma, 2020
Objective Cervical spine osteochondromas are rare with approximately 3% of solitary and 7-9% of hereditary osteochondromas occurring in the spine. Almost 50% of spinal osteochondromas occur in the cervical region.
R Botchu
exaly   +2 more sources

Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas [PDF]

open access: yesScientific Reports, 2013
Multiple osteochondromas is an autosomal dominant skeletal disorder characterized by the formation of multiple cartilage-capped tumours. Two causal genes have been identified, EXT1 and EXT2, which account for 65% and 30% of cases, respectively.
Anton, J.   +14 more
core   +2 more sources

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