Results 21 to 30 of about 2,295 (157)

Hereditary Multiple Exostoses: Current Insights [PDF]

open access: yesOrthopedic 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   +4 more
doaj   +2 more sources

Hereditary multiple osteochondromas in a child: a case report and discussion of postoperative complication management [PDF]

open access: yesFrontiers in Surgery
BackgroundThe pathogenesis of hereditary multiple exostoses is mainly related to genetic variants and often requires surgical resection when it causes clinical symptoms.
Haiting Jia, Yuting Wang, Tao Liu
doaj   +2 more sources

Congenital multiple exostoses with congenital heart disease

open access: yesMedical Journal of Dr. D.Y. Patil University, 2017
Multiple exostoses are a rare disorder. It is estimated to occur in 1; 50,000 pregnancies. It presents within the first decade of life and it has an autosomal mode of inheritance; though it has been associated with a spontaneous mutation in 10% of cases.
Ibrahim Aliyu, Teslim O Lawal
doaj   +2 more sources

Hereditary Multiple Exostoses with Rare Ocular Finding: A Case Report

open access: yesJournal of Current Ophthalmology
Purpose: To study rare ocular findings in a rare case of hereditary multiple exostoses (HME) and to study HME in one family. Methods: HME is an autosomal dominant genetic disease characterized by the presence of multiple exostoses (osteochondromas).
Shashi Tanwar   +3 more
doaj   +2 more sources

Spinal stenosis frequent in children with multiple hereditary exostoses

open access: yesJournal of Children's Orthopaedics, 2013
Purpose Children with multiple hereditary exostoses (MHE) have numerous osteochondromas, with the most prominent lesions typically over the appendicular skeleton.
Ali Ashraf   +5 more
doaj   +2 more sources

Hereditary multiple exostoses in a15-year-old boy: A case report and review of literature

open access: yesNigerian Journal of Paediatrics, 2016
Background: Hereditary Multiple Exostoses (HME) is a rare bone disease, usually associated with deformity and pressure symptoms. It is an autosomal dominant disorder characterized by the development of benign tumours growing outward from the metaphyses ...
Eke GK , Omunakwe HE , Echem RC
doaj   +4 more sources

Multiple hereditary exostoses: A pseudoaneurysm masquerading as tumor. [PDF]

open access: yesJ Radiol Case Rep, 2016
Multiple hereditary exostoses is an autosomal dominant condition characterized by numerous benign osteochondromas. Complications are rare and can include deformity, growth abnormality, fracture, adventitial bursa formation, local mass effect on a nerve ...
Trivedi H   +4 more
europepmc   +2 more sources

C2 intraspinal osteochondroma causing spinal cord compression in a patient with multiple hereditary exostoses

open access: yesIndian Spine Journal, 2022
Intraspinal osteochondroma causing neurological manifestations is a rare condition and can present as either solitary osteochondroma or more commonly as a part of multiple hereditary exostoses. We report a case of osteochondroma arising from lamina of C2
Janardhana P Aithala
doaj   +1 more source

Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study [PDF]

open access: yes, 2004
We performed a prospective genotype-phenotype study using molecular screening and clinical assessment to compare the severity of disease and the risk of sarcoma in 172 individuals (78 families) with hereditary multiple exostoses.
Monaco, AP   +12 more
core   +1 more source

Forearm deformities in children with hereditary multiple exostosis (review of literature) [PDF]

open access: yesГений oртопедии, 2020
Introduction Hereditary multiple exostoses, according to different authors, account for 16.0 to 43.0 % of all the cases of tumors, tumor-like and dysplastic diseases of the pediatric skeleton.
Alexander P. Pozdeev   +2 more
doaj   +1 more source

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