A child having rare Hereditary Multiple Exostosis with Covid-19 disease: A case study [PDF]
, 2022 : Hereditary Multiple Exostosis is a rare bone disease in pediatric age group. It is an autosomal dominant disorder, characterized by excessive bony overgrowth arising from lateral aspect of metaphysis of long bone, covered by a cartilaginous cap.
Hasnat, F +3 more
core +2 more sources
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 +3 more
doaj +1 more source
Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses [PDF]
, 2015 Las formas hereditarias de exostosis múltiple, actualmente denominada EXT1/EXT2-CDG dentro de los desórdenes congénitos de la glicosilación, son los tumores óseos benignos más comunes y se caracterizan por la formación de lesiones óseas cubiertas de ...
Asteggiano, Carla Gabriela +11 more
core +1 more source
Chest pain caused by multiple exostoses of the ribs: A case report and a review of literature [PDF]
, 2017 The aim of this paper is to report an exceptional case of multiple internal exostoses of the ribs in a young patient affected by multiple hereditary exostoses (MHE) coming to our observation for chest pain as the only symptom of an intra-thoracic ...
Calderaro, Cosma +8 more
core +1 more source
Mutational Analysis of EXT1in a Chinese Family Affected by Hereditary Multiple Osteochondroma [PDF]
BioMed Research International, 2021 Objectives. To discuss the mutational features and their relationships with disease in a family with hereditary multiple osteochondroma (HMO) from Guangxi Province (GXBB‐1 family), China. Methods. Genomic DNA and total mRNA were extracted from peripheral blood cells of GXBB‐1 family members.
Guangzhi Yuan +6 more
openaire +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 +4 more
doaj +1 more source
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 +3 more
doaj +1 more source
Reconstruction of the Hip in Multiple Hereditary Exostoses
Children, 2021 The hip joint involvement in multiple hereditary exostoses (MHE) occurs in 30–90%, causing pain and limitation of motion by femoroacetabular impingement, coxa valga, acetabular dysplasia, hip joint subluxation, and osteoarthritis.
Dong Hoon Lee, Dror Paley
doaj +1 more source
A case report on surgical excision of intracapsular osteochondroma of femur neck using medial approach without hip dislocation in a young male [PDF]
, 2023 Osteochondromas also called exostosis are commonest benign bone tumours. Traditionally Osteochondroma are considered as developmental malformations rather than true neoplasms and are thought to formed inside the periosteum due to separation of small ...
Bagimani, Pramod +5 more
core +2 more sources
A 40-Year-Old Male Presenting with Hereditary Multiple Exostosis: Management and Considerations
Case Reports in Orthopedics, 2019 Hereditary multiple exostosis is a rare condition in which numerous benign osteochondromas form throughout the body, typically in areas of high bone turnover such as the metaphyseal plates of long bones.
Matthew Wells, Zackary Birchard
doaj +1 more source