Results 91 to 100 of about 713 (172)

Hereditary Multiple Exostoses (HME) with Peroneal Nerve Compresion: A Case Report

International Journal of Medical Physics, Clinical Engineering and Radiation Oncology, 2023
Onarisa Ayu, Muhammad Iqbal
openaire   +1 more source

Large osteochondroma excision from distal radius [PDF]

Osteochondroma is a common benign bone tumor, originating within the periosteum as a small cartilaginous nodule. The distal femur, the proximal tibia, and the proximal humerus are the most common locations and the majority of these lesions cause no ...
Desai, Sarvang, Gupta, Vatsal A., Katkani, Anmol, Modi, Lomesh P., Tomar, Aman   +4 more
core   +2 more sources

Unsuspected osteochondroma-like outgrowths in the cranial base of Hereditary Multiple Exostoses patients and modeling and treatment with a BMP antagonist in mice.

PLoS Genetics, 2017
Hereditary Multiple Exostoses (HME) is a rare pediatric disorder caused by loss-of-function mutations in the genes encoding the heparan sulfate (HS)-synthesizing enzymes EXT1 or EXT2.
Sayantani Sinha, Christina Mundy, Till Bechtold, Federica Sgariglia, Mazen M Ibrahim, Paul C Billings, Kristen Carroll, Eiki Koyama, Kevin B Jones, Maurizio Pacifici   +9 more
doaj   +1 more source

Pedunculated Osteochondroma of the Right Foot Following Traumatic Injury: A Rare Case Report [PDF]

Osteochondromas are the most common benign bone tumors, accounting for 20-50% of all benign osseous neoplasms. However, osteochondromas involving the foot and ankle are rare, representing only 3-10% of all cases.
Al Hakim, Muhammad Fariz, Pandelima, Maksum   +1 more
core   +2 more sources

Higher femoral head–to–femoral neck ratio are associated with limited range of motion of hip joints in hereditary multiple exostosis patients

Medicine Science
Hip involvement is one of the most common skeletal manifestations of hereditary multiple exostoses (HME) in 30-90% of the patients. The anatomical changes in the proximal femur in patients with HME, may lead to deformities and related functional deficits.
Mustafa Alper Incesoy, Osman Emre Aycan, Alper Koksal   +2 more
doaj   +1 more source

Growth modulation in genu valgum secondary to multiple hereditary exostosis [PDF]

Hereditary Multiple Exostoses (HME) is a rare disease with a prevalence of 1:50,000, which can manifest in various ways. This cartilaginous tumor can appear in a spectrum, ranging from mobility restriction to chronic pain and alignment disorders ...
Ismail, Imma Isniza, Kamisan, Norazian, Tharmaseelan, Shival   +2 more
core   +1 more source

A Solitary Osteochondroma Originating from the Spinous Process of the Third Cervical Vertebra: A Case Report and Comprehensive Literature Review

Journal of Spine Practice
Background Osteochondroma is one of the most common solitary bone lesions. Multiple lesions are possible only in some genetic abnormalities, such as hereditary multiple exostoses (HME).
Jinan Mohammed Aljasem, Abdulaziz Yousef Alahmed, Osama Abdullah Barnawi, Ghaida Ali Aljdhaa, Abdullah Salem Almalki, Ahmed Bin Ali Albinali, Ali Hussain Dallak, Jehad Mahmoud Ahmed, Abdullah Qaddah Alqahtani   +8 more
doaj   +1 more source

Ptpn11 Deletion in A Novel Cartilage Cell Causes Metachondromatosis by Activating Hedgehog Signaling [PDF]

, 2013
SHP2, encoded by PTPN11, is required for survival, proliferation and differentiation of various cell types1,2. Germ line activating mutations in PTPN11 cause Noonan Syndrome, while somatic PTPN11 mutations cause childhood myeloproliferative disease and ...
Wu, Qian
core   +1 more source

Hereditary Multiple Exostoses HME of the Spine; is Really a Benign Bone Tumour Syndrome? Editorial

Orthopedic & Muscular System, 2013
LANDI, ALESSANDRO, MANCARELLA, CRISTINA, DELFINI, Roberto   +2 more
openaire   +3 more sources

Developmental aspects of the trichorhinophalangeal syndromes [PDF]

, 2008
Langer-Giedion syndrome (LGS), also known as trichorhinophalangeal syndrome type II (TRPS II), and trichorhinophalangeal syndrome type I (TRPS I) are related conditions that result from deletions in chromosomal region 8q24.l l-q24.13.
Johnston, Tamra Lynn
core   +1 more source