Results 181 to 190 of about 6,285,374 (227)

Gene Variants Characterize and Distinguish Osteochondromas in Patients With Hereditary Multiple Osteochondromas

Journal of Orthopaedic Research
Hereditary Multiple Osteochondromas (HMO) is a rare, pediatric skeletal disorder characterized by osteochondromas that form along the growth plates. These benign tumors can cause skeletal deformities, joint dysfunction, chronic pain and other health ...
Christina Mundy, Sadhana Ramesh, Caroline Kim, Divya Talwar, Maurizio Pacifici, A. Arkader   +5 more
semanticscholar   +1 more source

THE UNUSUAL PRESENTATION OF EXCESSIVE SPURS LIKE OSTEOCHONDROMAS IN AN ADOLESCENT WITH HEREDITARY MULTIPLE OSTEOCHONDROMAS

International journal of scientific research, 2022
Hereditary Multiple Osteochondromatosis (HMO) is characterised by the presence of multiple osteochondromas, mainly affecting the long bones. Osteochondromas are bony projections that are either sessile or pendulated in form.
N. Laliotis, C. Chrysanthou, Panagiotis Konstandinidis   +2 more
semanticscholar   +1 more source

Multiple Osteochondromas: Case 4

2021
The patient is a 3-year-old boy. He presented with multiple masses around the right shoulder.
Xiaoguang Cheng, Yongbin Su, Mingqian Huang   +2 more
openaire   +1 more source

Scintigraphic Findings of Multiple Osteochondromas

Clinical Nuclear Medicine, 1986
Multiple osteochondromas (hereditary multiple exostoses, diaphyseal aclasis, cartilagenous exostoses) are anomalies of bone development in which multiple cartilagenous exostoses grow out from the cortical surface, mainly involving ends of the long bones.
W J, Shih, C N, Riley, P A, Domstad, F H, DeLand   +3 more
openaire   +2 more sources

Novel Mutations in Chinese Patients with Multiple Osteochondromas Identified Using Whole Exome Sequencing

Genetic Testing and Molecular Biomarkers, 2021
Background: Multiple osteochondromas (MO) are an autosomal-dominant disease characterized by the growth of multiple cartilage-capped prominences in the growth plate region of the metaphysis in long and flat bones. Materials and Methods: To detect genetic
Yu Tong, Junchao Luo, Yin Zhang, Zheping Hong, Li Cao, Xinji Chen, Jihang Chen, Q. Bi   +7 more
semanticscholar   +1 more source

Reliability of the Masada Classification for Forearm Involvement in Patients With Hereditary Multiple Osteochondromas (HMO)

Journal of pediatric orthopedics, 2022
Background: Classifications describing forearm lesions in patients with Hereditary Multiple Osteochondromatosis (HMO) have been used to recommend surgical intervention and stratify outcomes; however, there is no consensus on which classification offers ...
Maria F. Canizares, L. Wall, A. V. Van Heest, Suzanne Steinman, M. James, P. Miller, C. Vuillermin   +6 more
semanticscholar   +1 more source

Muenke Syndrome Associated With Multiple Osteochondromas

Journal of Craniofacial Surgery, 2012
Muenke syndrome caused by the FGFR3 Pro250Arg mutation is associated with craniosynostosis, hearing loss, and various bony anomalies. Although this mutation is involved in bone growth and development, bony tumors are rare in this condition. We describe a patient with a molecular diagnosis of Muenke syndrome who also presented with multiple ...
Simon G, Talbot, Joseph, Upton, Gary F, Rogers   +2 more
openaire   +2 more sources

Identification of Novel Mutations in the EXT1 and EXT2 Genes of Chinese Patients with Hereditary Multiple Osteochondromas

Genetic Testing and Molecular Biomarkers, 2021
Aim: To detect mutations in the EXT1 and EXT2 genes in four Chinese families with hereditary multiple osteochondromas (HMO). HMO is an autosomal dominant disorder characterized by the overgrowth of multiple cartilage-capped bones in the metaphysis of ...
Yu Tong, Yin Zhang, Junchao Luo, Zheping Hong, Xinji Chen, Q. Bi   +5 more
semanticscholar   +1 more source

A probable case of multiple osteochondromas in a Qing period (1644–1911) individual from Shandong, China

International Journal of Osteoarchaeology
This article aims to understand the impact of a condition causing multiple benign neoplasms on a historical individual, and increase understanding of disease processes using a paleopathological case.
Yawei Zhou, Fanhao Xi, Fangchao Zhao, Elizabeth Berger   +3 more
semanticscholar   +1 more source

Multiple Osteochondromas: An Incidental Finding

Journal of Diagnostic Medical Sonography, 2008
Multiple osteochondromas were detected during a lower extremity sonographic examination of a child with a palpable mass. An osteochondroma is a benign bone tumor that typically arises from the long bones, especially around the knee. Diagnosis is usually made during adolescence when a mass is palpated.
Brooke Weinrich, Kim Michael
openaire   +1 more source