Results 41 to 50 of about 1,805 (231)

Genetic analysis of seven pateints with Hereditary Multiple Osteochondromas (HMO). [PDF]

Am J Transl Res, 2022
Ren Z, Yuan JY, Zhang J, Tan Y, Chen WQ, Zhang ZT, Li YZ.   +6 more
europepmc   +2 more sources

Palovarotene for patients with multiple hereditary exostosis: results of MO-Ped, a terminated, randomized, placebo-controlled, double-blind phase 2 trial [PDF]

Scientific Reports
A phase II trial (MO-Ped; NCT03442985) assessed palovarotene in pediatric patients with multiple hereditary exostosis (MHE). Patients aged ≤ 14 years with MHE were randomized 1:1:1 to placebo, palovarotene 2.5 mg, or palovarotene 5.0 mg daily.
Luca Sangiorgi, Ernest U. Conrad, Fei Shih, Andrew Strahs, David S. Feldman   +4 more
doaj   +2 more sources

Identification of a rare case of intra-articular osteochondroma manifesting as three loose bodies in a patient with hereditary multiple osteochondromas: A case report. [PDF]

Oncol Lett, 2015
Kong M, Cao LI, Zhang Q, Fang Y, Zhao C, Gu H, Zhang S, Chen YU, Wu J, Bi Q.   +9 more
europepmc   +3 more sources

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

, 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.
Flohr, Stefan, Gomez, Santiago, Kierdorf, Horst, Kierdorf, Uwe, Miller, Karl V.   +4 more
core   +5 more sources

Pseudoaneurysm Complicating Proximal Humeral Exostosis: A Case Report of a Missed Diagnosis on Computed Tomography Angiographic Examination

Case Reports in Orthopedic Research, 2022
Vascular complications of osteochondromas of the humerus are extremely rare. Only 9 cases with pseudoaneurysms of the brachial artery complicating osteochondromas of the humerus were reported in 7 English articles.
Ashraf A. Khanfour, Ahmed S. Gaweesh, Tamer Y. Gaweesh   +2 more
doaj   +1 more source

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

, 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., Armstrong, J., Artuch, R., Asteggiano, Carla Gabriela, Balcells, S., Delgado, María Andrea, Grinberg, D., Lapunzina, P., Martorell, L., Nevado, J., Sangorrin, A., Sarrión, P., Torner, F., Urreizti, R., Vilaseca, M. A.   +14 more
core   +4 more sources

Ventral Scapular Osteochondroma in Hereditary Multiple Exostosis

Annals of Thoracic Surgery Short Reports, 2023
Hereditary multiple exostosis is a rare, autosomal dominant, highly penetrant genetic disorder characterized by the development of osteochondromas on the metaphysis of long and flat bones. The development of osteochondromas on the scapula is unusual but has been reported.
Gregory P. Mouradian, Sam Hong, Emmanuel Daon   +2 more
openaire   +1 more source

Operative Treatment of Deformities of the Forearm in Hereditary Multiple Osteochondromas [PDF]

Journal of the Korean Orthopaedic Association, 1994
Kie Bong Wang, Hui Taek Kim, Kuen Tak Suh, Chong Il Yoo   +3 more
openalex   +2 more sources

Two Siblings Followed Up for Hereditary Multiple Exostoses

Haseki Tıp Bülteni, 2014
Hereditary multiple exostoses is an autosomal dominant disease with abnormal bone formation especially at the long bones. Osteochondromas, which occur in the course of the disease, can cause growth disturbances in affected children.
Meltem Erol, Özgül Yiğit, Oktay Adanır, Mehmet Toksöz, Halis Narin, Veysel Gök, Dilek Borakay, Murat Konya   +7 more
doaj   +1 more source

In Situ Hybridization of Feline Leukemia Virus in a Case of Osteochondromatosis

Veterinary Sciences, 2022
Osteochondromatosis, also known as multiple cartilaginous exostosis, polyostotic osteochondroma, and multiple osteochondromas, comprises one-fifth of all primary bone tumors in cats, with no breed or sex predisposition or hereditary pattern.
Anna Szilasi, Zsófia Koltai, Lilla Dénes, Gyula Balka, Míra Mándoki   +4 more
doaj   +1 more source