Results 1 to 10 of about 288 (135)
Diaphyseal Aclasis With Pes Anserinus Syndrome. [PDF]
We describe the case of a 20-year-old man who presented with a bony swelling over the medial proximal tibia that caused pain along the pes anserinus tendons, and a history of multiple asymptomatic bony swellings. Wide extraperiosteal resection of the swelling relieved the symptoms with a good outcome within a year.
Tiwari V, Dwidmuthe S, Sahoo SS.
europepmc +6 more sources
An unusual example of hereditary multiple exostoses: a case report and review of the literature [PDF]
Background Hereditary multiple exostoses (HME) is a rare skeletal disorder characterised by a widespread. distribution of osteochondromas originating from the metaphyses of long bones. Case presentation This case study examines a 55-year-old male cadaver
Rebecca Chilvers +3 more
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The term 'diaphyseal achalasia' must be changed with the term 'diaphyseal aclasis'. [PDF]
Dear Editor, I have read the case report of Thomas et al with interest. The title of the report contains the term ‘diaphyseal achalasia’ to define multiple osteochondromatosis.1 This was also stated in the Introduction section.1 Multiple osteochondromatosis is also defined as ‘diaphyseal aclasis’.2 I would like to thank Thomas et al, however I ...
Çıtlak A.
europepmc +7 more sources
A family with diaphyseal aclasis and peripheral dysostosis. [PDF]
Autosomal dominant inheritance of a type of peripheral dysostosis occurred in a family with diaphyseal aclasis. The features of their type of peripheral dysostosis were short limbed short stature, normal intelligence, very stubby fingers, flat face and nose, shortened metacarpals and terminal phalanges, thickened beaten-copper skull vault, and advanced
Brooks AP, Wynne-Davies R.
europepmc +6 more sources
Spinal exostosis in a boy with multiple hereditary exostoses. [PDF]
We report on a 13‐year‐old boy who presented with multiple hereditary exostosis and had development of back pain, associated with neurological deficits, and was found to have exostoses in the spinal canal. Spine radiograph showed a cauliflower‐like abnormality of multiple exostoses of the posterior arch (pedicle) of the thoracic vertebrae (T3–5 ...
Al Kaissi A +3 more
europepmc +6 more sources
Hereditary Multiple Exostoses—A Review of the Molecular Background, Diagnostics, and Potential Therapeutic Strategies [PDF]
Hereditary multiple exostoses (HMEs) syndrome, also known as multiple osteochondromas, represents a rare and severe human skeletal disorder. The disease is characterized by multiple benign cartilage-capped bony outgrowths, termed exostoses or ...
Ewelina Bukowska-Olech +9 more
doaj +2 more sources
Current paediatric orthopaedic practice in hereditary multiple osteochondromas of the forearm: a systematic review [PDF]
Introduction: This systematic review aims to answer three research questions concerning the management of hereditary multiple osteochondromas of forearm in children: What is the best available evidence for the currently employed surgical procedures? What
EL-Sobky Tamer A. +5 more
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