Pain and Depression in Pediatric Hereditary Multiple Exostoses Patients
Acta Medica Alanya, 2019 Aim: In this study, we sought to evaluate the complications of Hereditary Multiple Exostosis (HME) particularly the presence of pain, and its effects on pediatric and adolescent groups.Patients and Methods: 72 (37male/32female) patients aging between 10 ...
Osman Emre Aycan
doaj +1 more source
Journal of Anatomy, Volume 247, Issue 3-4, Page 856-868, September/October 2025.Overview of XS of pathological radius. Using anatomical descriptions, CT scanning and bone histology, we investigate several skeletal overgrowths of bone (exostoses) in the skeleton of a jackal‐like canid from the world famous Langebaanweg, a Mio‐Pliocene locality in South Africa.
Anusuya Chinsamy, Alberto Valenciano
wiley +1 more source
Prognostic Factors in Dedifferentiated Chondrosarcoma: A Retrospective Analysis of a Large Series Treated at a Single Institution. [PDF]
, 2019 Background:Dedifferentiated chondrosarcomas (DDCSs) are highly malignant tumors with a dismal prognosis and present a significant challenge in clinical management.
Chebib, Ivan +10 more
core +1 more source
One-stage surgical excision of a huge bilateral multiple osteochondroma of the hip: a case report
Electronic Physician, 2017 Osteochondroma or hereditary multiple exostoses is the most common benign bone tumor and is usually found in young patients. Osteochondromata of the proximal femur or hip have been reported in 30% to 90% of patients with hereditary multiple exostoses ...
Afshin Taheriazam, Amin Saeidinia
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Radiological conference. Osteopoikilosis [PDF]
, 1998 published_or_final_versio
Peh, WCG, Wong, LLS
core
Spinal stenosis frequent in children with multiple hereditary exostoses
Journal 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 +1 more source
Familiäre Tumorerkrankungen im Knochen [PDF]
, 2018 Zusammenfassung: Familiäre Erkrankungen, die zur Bildung von Knochentumoren führen, sind selten. Sie entwickeln sich im Zusammenhang mit genetischen Alterationen, die den Zellzyklus (Retinoblastomsyndrom/RB1, Li-Fraumeni-Syndrom/p53), wachstumssteuernde ...
Baumhoer, D., Jundt, G.
core
Hereditary multiple exostoses in a15-year-old boy: A case report and review of literature
Nigerian 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
Importância do estudo multigénico no diagnóstico molecular de doenças raras por sequenciação de nova geração [PDF]
, 2019 Introdução: A sequenciação de nova geração (NGS) revolucionou o diagnóstico molecular das doenças raras (DR) proporcionando a análise de um maior número de genes, resultados mais rápidos e custos reduzidos. A NGS usando diferentes abordagens, possibilita
Gonçalves, João +4 more
core
A genotype-phenotype study of hereditary multiple exostoses in forty-six Chinese patients
BMC Medical Genetics, 2017 Background Hereditary multiple exostoses (HME) is a rare autosomal dominant skeletal disorder that can cause a variety of clinical manifestations.
Yuchan Li +4 more
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