Results 181 to 190 of about 1,621 (210)
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Journal of Pediatric Orthopaedics
Background: Hereditary multiple osteochondromas (HMO) is a common pediatric condition defined by multiple cartilage-capped bony lesions. Spinal osteochondromas affect up to 68% of HMO patients. Although most are asymptomatic, intraspinal osteochondromas can cause significant neurological symptoms and morbidity.
Jack Legler +9 more
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Background: Hereditary multiple osteochondromas (HMO) is a common pediatric condition defined by multiple cartilage-capped bony lesions. Spinal osteochondromas affect up to 68% of HMO patients. Although most are asymptomatic, intraspinal osteochondromas can cause significant neurological symptoms and morbidity.
Jack Legler +9 more
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Genetic screening of EXT1 and EXT2 in Cypriot families with hereditary multiple osteochondromas
Journal of Genetics, 2015The purpose of this study was to perform genetic screening of the exostosin 1 (EXT1) and exostosin 2 (EXT2) genes in Cypriot patients with a clinical diagnosis of hereditary multiple osteochondromas (HMO). Initially, mutation analysis of the EXT1 gene was performed by Sanger sequencing.
TANTELES, GEORGE A. +10 more
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Osteochondroma and Multiple Hereditary Exostosis
2022Krishna V. Suresh, Paul D. Sponseller
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A New Classification System for Forearm Deformities Caused by Hereditary Multiple Osteochondromas
The Journal of Hand SurgeryThe objective of this study was to evaluate the Masada and Jo classifications for clinical use in patients with forearm deformity caused by hereditary multiple osteochondroma and propose a new classification system that is all-inclusive and can guide clinical management.A retrospective review of 275 forearms was performed.
Chloe Xiaoyun Chan +6 more
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Osteochondroma with Cervical Cord Compression in Hereditary Multiple Exostoses
Spine, 1990S A, Shapiro, T, Javid, T, Putty
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[Molecular diagnosis and prenatal diagnosis in a hereditary multiple osteochondromas family].
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences, 2014To identify the mutation in the disease gene and provide prenatal diagnosis for a hereditary multiple osteochondromas (HMO) family.The exons of EXT1 gene in the proband with HMO and his family members were amplified by PCR. The products were analyzed by direct sequencing.
Ying, Tang +4 more
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Genetic testing in prostate cancer management: Considerations informing primary care
Ca-A Cancer Journal for Clinicians, 2022Veda N Giri +2 more
exaly
[Genetic diagnosis for a Chinese Han family with hereditary multiple osteochondromas].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 2014To identify the genetic cause for a Chinese Han family affected with hereditary multiple osteochondromas.Two patients, five unaffected relatives of the family and 100 unrelated healthy controls were collected. The coding sequences and intron/exon boundaries of EXT1 gene were amplified with polymerase chain reaction (PCR) and sequenced.A heterozygous c ...
Xue-shuang, Huang +4 more
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Multiple hereditary osteochondromas - A rare case
Journal of the Anatomical Society of India, 2017openaire +1 more source