Results 21 to 30 of about 1,873 (147)

A Novel Pathogenic Large Duplication in EXT1 Identified in a Family with Multiple Osteochondromas. [PDF]

Genes (Basel)
Multiple osteochondromas (MO) is an autosomal dominant disorder and the most common genetic skeletal dysplasia, characterized by the growth of bone outgrowths capped by cartilage, called osteochondromas.
Bartolotti I, Sobul K, Corsini S, Scognamiglio D, Moroni A, Gnoli M, Sangiorgi L, Pedrini E.   +7 more
europepmc   +2 more sources

An unusual diagnosis for an usual test

Italian Journal of Pediatrics, 2020
Background Hereditary multiple osteochondromas (HMO) is a genetic condition characterized by the presence of multiple osteochondromas, usually at the lateral side of the most active growth plate of a long bone.
Andrea Trombetta, Vanessa Migliarino, Flavio Faletra, Egidio Barbi, Gianluca Tornese   +4 more
doaj   +1 more source

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

Multiple osteochondromas (MO) [PDF]

, 2009
Review on Multiple osteochondromas (MO), with data on clinics, and the genes ...
Bovée, JVMG, JVMG Bovée, CMA Reijnders, Reijnders, CMA   +3 more
core   +1 more source

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

Bilateral scapulothoracic osteochondromas in a patient with hereditary multiple exostosis: a case report and review of the literature

Orthopedic Reviews, 2016
Hereditary multiple exostosis (HME) is an autosomal dominant disorder characterized by two or more benign growing, cartilage capped tumors of long bones called osteochondromas.
Markus Rupp, Jendrik Hardes, Michael J. Raschke, Adrian Skwara   +3 more
doaj   +1 more source

A Commentary on “Clinical and Functional Outcomes of Ulnar Lengthening in the Treatment of Masada Type I Forearm Deformities in Hereditary Multiple Osteochondromas”

Journal of Orthopedic and Spine Trauma, 2020
No abstract is available.
Alireza Moharrami, Hamid Arabi
doaj   +1 more source

Proximal clavicular osteochondroma: A report of an unusual site

Journal of Pediatric Surgery Case Reports, 2022
Background: Osteochondromas are benign surface tumors that comprise a large sum of all bone tumors. They can present as solitary lesions or part of a collective such as in hereditary multiple osteochondromas (HMO).
Motaip H. Alrawili, Rakan Aldusari, Samir Alsayegh, Faten Al Robian   +3 more
doaj   +1 more source

Deletion of exon 8 from the EXT1 gene causes multiple osteochondromas (MO) in a family with three affected members. [PDF]

, 2016
Multiple osteochondromas (also called hereditary multiple exostoses) is an autosomal dominant disorder characterized by multiple cartilaginous tumors, which are caused by mutations in the genes for exostosin-1 (EXT1) and exostosin-2 (EXT2).
Stefan Kuchen, Simon D. Gerber, Peter M. Villiger, Kuchen, Stefan, Villiger, Peter, Lei Zhuang, Zhuang, Lei, Trueb, Beat, Gerber, Simon D, Beat Trueb   +9 more
core   +1 more source