Results 101 to 110 of about 15,961 (249)

Small sharp exostosis tip in solitary osteochondroma causing intermittent knee pain due to pseudoaneurysm

open access: yes, 2014
Background: Complications of solitary or multiple osteochondromas are rare but have been reported in recent literature. Most reported complications arose in patients with multiple and/or sizable osteochondromas.
Bachhuber, D. (Dagmar)   +6 more
core   +1 more source

Pain, Physical and Social Functioning, and Quality of Life in Individuals with Multiple Hereditary Exostoses in the Netherlands [PDF]

open access: yes, 2012
Background: This study aimed to assess pain and quality of life in a large cohort of patients with multiple hereditary exostoses. Methods: All 322 known patients with multiple hereditary exostoses in the Netherlands were asked to participate.
Bulstra, S. K.   +4 more
core   +2 more sources

Three-dimensional printing and computer navigation assisted hemipelvectomy for en bloc resection of osteochondroma

open access: yesMedicine, 2017
Rationale: Three-dimensional (3D) printed templates can be designed to match an individual's anatomy, allowing surgeons to refine preoperative planning. In addition, the use of computer navigation (NAV) is gaining popularity to improve surgical accuracy ...
Yaqing Zhang   +5 more
semanticscholar   +1 more source

Variations in the Terminal Branches of the Brachial Plexus in the Axillary Fossa

open access: yesBioMed Research International, Volume 2025, Issue 1, 2025.
Background: The brachial plexus is the primary nerve source for the upper limb. Variations in its anatomy can alter the nerve supply to the upper extremity. Such deviations are clinically important, as they can change the symptomatology of various pathologic conditions, leading to misdiagnosis, inadequate treatment, and surgical failures as a ...
Elena Bozhikova   +5 more
wiley   +1 more source

Trigger finger due to phalangeal osteochondroma of an adult: A case report

open access: yesJournal of Orthopaedic Surgery, 2020
Trigger finger is stenosing tenosynovitis that occurs in A1 pulley. It usually occurs idiopathically in patients’ 40s and 50s. On the other hand, pediatric trigger finger usually occurs before 8 years old in pediatric patients.
Hoi Young Kwon, Hong Je Kang
doaj   +1 more source

Osteocondroma de apófisis coronoides [PDF]

open access: yes, 2006
El osteocondroma es la neoplasia benigna más común del esqueleto. En la cabeza se ha descrito su localización en base de cráneo, cara posterior del maxilar, senos maxilares, y en diferentes áreas de la mandíbula, como cóndilo, rama, cuerpo y región ...
Cornejo, Marco   +4 more
core   +1 more source

A Case of Proteus Syndrome, Suspected as Maffucci Syndrome in a Chinese Child

open access: yesCase Reports in Pediatrics, Volume 2025, Issue 1, 2025.
Proteus syndrome (PS) is an exceptionally rare disorder characterized by asymmetric and disproportionate overgrowth of connective tissues. We report the case of an 8‐year‐old female presenting with irregular cranial protrusion, bilateral supraorbital ridge enlargement, overgrowth of the right hand and left foot, and a pelvic MRI revealing an ovarian ...
Lin Juan   +6 more
wiley   +1 more source

Osteochondroma of the mandibular condyle: Resection and reconstruction using vertical sliding osteotomy of the mandibular ramus [PDF]

open access: yes, 2009
Osteochondroma is one of the most common benign bone tumours, although not in the craniofacial region. More than half of these appear in the coronoid process.
Escrig de Teigeiro, M.   +4 more
core  

Condylar Hyperplasia: An Updated Review of the Literature [PDF]

open access: yes, 2015
Condylar hyperplasia (CH) is a rare disorder characterized by excessive bone growth that almost always presents unilaterally, resulting in facial asymmetry. Classification of the different types of CH can differ depending on the authors.
Almeida, Luis Eduardo   +2 more
core   +2 more sources

Genetic counseling for congenital disorders of glycosylation (CDG)

open access: yesJournal of Genetic Counseling, Volume 33, Issue 6, Page 1358-1364, December 2024.
Abstract Congenital disorders of glycosylation (CDGs) are a genetically and clinically diverse group of disorders that arise as a result of defects within glycosylation synthetic pathways. CDGs are caused by pathogenic variants in many different genes in the glycosylation network.
Tara Weixel   +2 more
wiley   +1 more source

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