Prevalence of Oral Alterations and Correlation Between Oral and Cutaneous Neurofibromas in Neurofibromatosis Type 1: A Retrospective Case-Control Study. [PDF]
J Oral Pathol MedABSTRACT Objective The aim of this study was to determine the prevalence of oral alterations detectable through physical examination in NF1 individuals. Additionally, we assessed the correlation between the number of oral and cutaneous neurofibromas. Design This retrospective study evaluated oral alterations in individuals with and without NF1.
de Pinho Montovani P +3 more
europepmc +2 more sources
Eccentric Training as an Adjunct to Rehabilitation Program for Hereditary Multiple Exostoses: A Case Report [PDF]
Journal of Clinical and Diagnostic Research, 2016 Hereditary multiple exostoses an autosomal dominant skeletal disorder characterized by multiple cartilage-capped benign exostoses that typically occur in the metaphysis of long bones.
Zeynep Hazar Kanik +4 more
doaj +1 more source
Multiple Heriditary Exostoses in a Family for Three Generation of Indian Origin with Review of Literature [PDF]
Journal of Clinical and Diagnostic Research, 2014 Multiple hereditary exostoses (MHE) are an autosomal dominant disorder, consisting of multiple cartilage capped bone tumour arising from the metaphysis of long tubular bones. Mutations are seen in Exostosin-1 and Exostosin-2 genes.
Kalyani R +4 more
doaj +1 more source
Indian 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
Hereditary multiple exostoses: A case report and literature review
SAGE Open Medical Case Reports, 2022 Osteochondroma is the most common bone tumor representing 20%–50% of all benign bone tumors and 10%–15% of all bone tumors. Osteochondroma has similar radiological appearance in both solitary and multiple forms; the latter is an autosomal dominant ...
Thi Hien Ha +6 more
doaj +1 more source
Clinical and radiological characteristics of forearm deformities in children with multiple hereditary exostoses [PDF]
Гений oртопедии, 2019 Introduction The incidence of forearm deformities in children with multiple hereditary exostoses (MHE) ranges from 30 to 80 %. There are few studies of deformities of the forearm in MHE patients in the literature that describe not only the location of ...
Ekaterina A. Zakharyan +2 more
doaj +1 more source
Hereditary Multiple Exostoses with Ulnar Hemimelia
Proceedings, 2021 Hereditary Multiple Exostoses is a skeletal dysplasia that is very rare and defined by formation of numerous cartilage capped benign tumours either pedunculated or sessile known as osteochondromas throughout skeleton especially around the growth plates ...
Syed Wasif Ali Shah +5 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. +14 more
core +4 more sources
Forearm deformities in children with hereditary multiple exostosis (review of literature) [PDF]
Гений 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