Results 31 to 40 of about 1,132 (155)
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
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Bone deformities with hereditary multiple osteochondromas [PDF]
Danish Medical JournalINTRODUCTION. Hereditary multiple osteochondromas (HMO) is a genetic skeletal disorder caused by defects in exostosin glycosyltransferase 1 (EXT1) or 2 (EXT2) genes. It develops mainly in the growth period and causes multiple osteochondromas (OC) in the physis of the long bones, leading to discomfort and deformities. This study aimed to investigate the
Brink Petersen, Rikke +3 more
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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
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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
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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
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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
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Frontiers in Genetics, 2021 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
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Foramen magnum osteochondroma causing myelopathy in a patient with hereditary multiple exostoses [PDF]
Surgical Neurology International, 2020 Background: Osteochondromas are commonly occurring benign bone tumors which may be either a solitary lesion or occur due to association with hereditary multiple exostoses (HMEs). There have been several reported cases of spinal osteochondromas, but intracranial lesions are rare.
Sinha, Siddharth +2 more
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A patient with novel mutations causing MEN1 and hereditary multiple osteochondroma [PDF]
Endocrinology, Diabetes & Metabolism Case Reports, 2015 Summary We report of a male patient aged 32 years who presented with primary hyperparathyroidism. Three parathyroid glands were resected. At the age of 46 years, nervus facialis irritation was noted, and an MRI scan incidentally revealed a non-functioning pituitary adenoma with affection of the chiasma opticum.
Remde, Hanna +3 more
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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
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