Results 21 to 30 of about 1,261 (184)

Reconstruction of the Hip in Multiple Hereditary Exostoses [PDF]

Children, 2021
The hip joint involvement in multiple hereditary exostoses (MHE) occurs in 30–90%, causing pain and limitation of motion by femoroacetabular impingement, coxa valga, acetabular dysplasia, hip joint subluxation, and osteoarthritis.
Dong Hoon Lee, Dror Paley
doaj   +2 more sources

Popliteal artery pseudoaneurysm caused by non–penetrating trauma in a patient with hereditary multiple osteochondromatosis [PDF]

Radiology Case Reports, 2022
Hereditary multiple osteochondromatosis is a genetic condition characterized by the appearance of numerous osteochondromas, which can cause pseudoaneurysms in rare cases.
Oscar Andrés Parada Duarte, MD, Juan Guillermo Arámbula Neira, MD, Valeria del Castillo Herazo, MD, María Fernanda Oviedo Lara, MD, Adriana Lucía López Polanco, MD, Andrés Felipe Durán Omaña, MD, Andrés Felipe Herrera Ortiz, MD   +6 more
doaj   +3 more sources

Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas [PDF]

Therapeutics and Clinical Risk Management, 2016
Susan Akbaroghli,1,* Maryam Balali,2,* Behnam Kamalidehghan,3,4 Siamak Saber,4 Omid Aryani,5 Goh Yong Meng,6 Massoud Houshmand4 1Mofid Children’s Hospital, Shahid Beheshti University of Medical Sciences, 2ENT and Head & Neck Research Center ...
Akbaroghli S, Balali M, Kamalidehghan B, Saber S, Aryani O, Yong Meng G, Houshmand M   +6 more
doaj   +1 more source

Dysplasia epiphysealis hemimelica: A histological comparative study with osteochondromas [PDF]

Journal 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, T. J. M. Welting, A. M. Witlox, L. W. van Rhijn, H. M. Staal   +4 more
doaj   +2 more sources

Cervical Myelopathy Due to an Osteochondroma in Multiple Hereditary Exostosis

Case Reports in Orthopedics
Hereditary multiple exostosis is a rare genetic condition characterized by the development of multiple exostoses. Vertebral localization is rare, less than 7%. Spinal cord compression in hereditary multiple exostosis is a rare condition. We report the case of a 22‐year‐old man with cervical spinal cord compression due to an osteochondroma with ...
Géraud Garcia Segbedji, Cédric Dongmo Mayopa, Xavier Banse, Pierre-Louis Docquier   +3 more
openaire   +2 more sources

Surgical Approach and Considerations for Compressive Thoracic Intraspinal Osteochondroma in Familial Hereditary Multiple Exostosis [PDF]

Diseases
Introduction: Hereditary multiple exostosis or hereditary multiple osteochondromas is a very rare clinical condition. Usually, these lesions tend to occur in the pediatric population, remaining silent until adulthood.
Corneliu Toader, Antonio-Daniel Corlatescu, Nicolaie Dobrin, Razvan-Adrian Covache-Busuioc, Horia Petre Costin, Alexandru Vlad Ciurea   +5 more
doaj   +2 more sources

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

BMC 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, James A. Gallagher, Nathan Jeffery, Alistair P. Bond   +3 more
doaj   +2 more sources

Metachondromatosis: More than just multiple osteochondromas [PDF]

Journal of Children's Orthopaedics, 2013
Introduction Metachondromatosis is a rare genetic disease of osteochondroma and enchondroma formation, caused by loss of function of the PTPN11 gene. It is distinct from other similar conditions such as multiple osteochondromas and hereditary multiple ...
Thomas J. Fisher, Nicole Williams, Lloyd Morris, Peter J. Cundy   +3 more
doaj   +2 more sources

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

Frontiers in Pediatrics, 2023
Xuejun Zhang, Fan Jingyi, Li Chengxin
exaly   +2 more sources

Spontaneous Regression of Multiple Osteochondromas in a Patient With Hereditary Multiple Exostoses: A Case Report. [PDF]

Cureus
Hereditary multiple exostoses (HME) is an autosomal dominant disorder characterized by the development of multiple osteochondromas, primarily near the metaphyses of long bones. We report a case of HME in which multiple symptomatic lesions showed spontaneous regression. The patient was an 11-year-old boy with osteochondromas involving both distal femurs
Ikeda K, Teruya S, Tsuge H, Onishi S.
europepmc   +3 more sources