Results 101 to 110 of about 1,639 (208)

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

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  

Treatment of Ewing Sarcoma, Paediatric Bone Sarcomas and Severe Paediatric Spinal Deformities in Finland [PDF]

, 2017
Background: Ewing sarcomas are rare highly malignant tumours. There are not many population-based studies including both bone and soft tissue tumours. Previous reports have suggested that the incidence of Ewing sarcoma in the paediatric population may be
Serlo, Joni
core  

Rare Case Report: Chondrosarcoma Arising from Osteochondroma in MHE patient. [PDF]

, 2015
This is a unique case of chondrosarcoma. From this case, we learn that, Multiple Hereditary Exostoses have strong connection with familial bond. This disease has male predominance, but in this case, the family don’t have any son, and the father are ...
Hartanta, Sutiansi, Simanjuntak, Charles A   +1 more
core   +3 more sources

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

Surg Neurol Int, 2023
Silva JE, Monteiro GA, Silva STE, Bezerra GMDS, Cavalcante-Neto JF, Bezerra DA, Vasconcelos JLM, Leal PRL.   +7 more
europepmc   +1 more source

Solitary Osteochondroma Arising from the Dorsal Vertebral Spinous Process [PDF]

, 2014
Introduction: Osteochondroma are benign tumors which arise from aberrant cartilage nodules within the periosteum. They can be either pedunculated or sessile and are more common in the extremities and rarely seen in spine.
Joshi, Ruban Raj, Sundararaj, Gabriel David   +1 more
core   +3 more sources

Radiological conference. Paget's disease [PDF]

, 1998
published_or_final_versio
Ching, ASC, Peh, WCG
core  

Hereditary Multiple Exostoses: Current Insights

Orthopedic Research and Reviews, 2019
Antonio D’Arienzo, Lorenzo Andreani, Federico Sacchetti, Simone Colangeli, Rodolfo Capanna Department of Translational Research on New Surgical and Medical Technologies, University of Pisa, Pisa, ItalyCorrespondence: Federico SacchettiDepartment of
D'Arienzo A, Andreani L, Sacchetti F, Colangeli S, Capanna R   +4 more
doaj  

A special type hereditary multiple osteochondroma in patients with proximal ulna osteochondroma

Abstract Background: Hereditary Multiple Osteochondroma (HMO) is a rare condition that frequently impacts the forearm and results in radial head dislocation. Consequently, orthopedic surgeons prioritize prognostication of factors contributing to radial head dislocation and implementing preventive measures.
An Yan, Miao Li, Xiaoqian Tan, Qian Tan, Weihua Ye, Jiangyan Wu, Haibo Mei, Guanghui Zhu, Han Xiao   +8 more
openaire   +1 more source

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

Front Pediatr, 2023
Fan J, Zhang X, Sun L, Li C, Qi X, Sun B.   +5 more
europepmc   +1 more source

Hereditary multiple exostoses: an educational review

Insights into Imaging
Hereditary multiple exostoses (HME), an autosomal dominant disorder with an incidence of 1:50,000 to 1:100,000, is characterised by the formation of multiple osteochondromas arising from the metaphyses of long and flat bones.
Alvaro Rueda-de-Eusebio, Sara Gomez-Pena, María José Moreno-Casado, Gloria Marquina, Juan Arrazola, Ana María Crespo-Rodríguez   +5 more
doaj   +1 more source