Results 61 to 70 of about 3,566 (172)

Two Siblings Followed Up for Hereditary Multiple Exostoses

Haseki Tıp Bülteni, 2014
Hereditary multiple exostoses is an autosomal dominant disease with abnormal bone formation especially at the long bones. Osteochondromas, which occur in the course of the disease, can cause growth disturbances in affected children.
Meltem Erol, Özgül Yiğit, Oktay Adanır, Mehmet Toksöz, Halis Narin, Veysel Gök, Dilek Borakay, Murat Konya   +7 more
doaj   +1 more source

Do plantar calcaneal spurs make the plantar aponeurosis enthesis stronger? A biomechanical analysis

Journal of Anatomy, Volume 248, Issue 4, Page 591-597, April 2026.
Novel testing set up for determining enthesial avulsion parameters. Donor calcanei were dissected to isolate the central band of the plantar fascia, and mounted in a custom 3D‐printed rig (Fig A, B, C) for uniaxial tensile testing of the plantar fascia enthesis (Fig D). This study demonstrated no significant differences in the avulsion parameters, Fmax
Joanna Tomlinson, Kai Chun Li, Johann Zwirner   +2 more
wiley   +1 more source

Pathogenesis and potential therapeutic targets of trichorhinophalangeal syndrome; lessons obtained from animal studies

Developmental Dynamics, Volume 255, Issue 3, Page 228-245, March 2026.
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki, Rinna Kanai, Sayuri Tatsuta, Shinichi Kawaguchi, Masatsune Itoh, Shinsuke Ohba, Makoto Abe   +6 more
wiley   +1 more source

Carpal sheath hernia in a cob: Unusual case, unorthodox fix

Equine Veterinary Education, Volume 38, Issue 5, Page 239-242, May 2026.
A. Hawkins, R. Smith
wiley   +1 more source

Coronal malalignment of lower legs depending on the locations of the exostoses in patients with multiple hereditary exostoses

BMC Musculoskeletal Disorders, 2019
Backgrounds Though malalignment of lower legs is a common pathologic phenomenon in multiple hereditary exostoses (MHE), relationship between locations of exostoses and malalignment of lower legs remains unclear.
Yeong Seub Ahn, Seong Hwan Woo, Sung Ju Kang, Sung Taek Jung   +3 more
doaj   +1 more source

Multiple Hereditary Exostoses [PDF]

HSS Journal®: The Musculoskeletal Journal of Hospital for Special Surgery, 2005
Carolyn M, Sofka, Gregory R, Saboeiro, Robert, Schneider   +2 more
openaire   +2 more sources

Hemothorax caused by vertebral exostoses

The Pan African Medical Journal, 2019
Spontaneous hemothorax is a rare condition and sometimes occurs during anticoagulant therapy for venous thromboembolism. Other causes of the condition are bleeding disorders, complication of spontaneous pneumothorax and pleural malignancy.
Jamel EL Ghoul, Soued Ferjani
doaj   +1 more source

Popliteal artery pseudoaneurysm and secondary ipsilateral deep vein thrombosis caused by an exostosis in a mature adult

Journal of Vascular Surgery Cases and Innovative Techniques
Exostosis (also known as osteochondroma) is the most common benign bony lump of young people, usually arising at the distal femur. Vascular complications associated with exostoses are rare and include true aneurysm or pseudoaneurysm formation, deep vein ...
He Huang, MM, Xiaosong Zhang, MM, Yusheng Wang, MM, Hao Tang, MM, Xiaoming Huang, BM, Honggang Zhang, MD, Da Li, MD   +6 more
doaj   +1 more source

Hereditary multiple exostoses in a15-year-old boy: A case report and review of literature

Nigerian Journal of Paediatrics, 2016
Background: Hereditary Multiple Exostoses (HME) is a rare bone disease, usually associated with deformity and pressure symptoms. It is an autosomal dominant disorder characterized by the development of benign tumours growing outward from the metaphyses ...
Eke GK , Omunakwe HE , Echem RC
doaj  

Hereditary multiple exostoses caused by a chromosomal inversion removing part of EXT1 gene. [PDF]

Mol Cytogenet, 2023
Alexandrou A, Salameh N, Papaevripidou I, Nicolaou N, Myrianthopoulos P, Ketoni A, Kousoulidou L, Anastasiou AM, Evangelidou P, Tanteles GA, Sismani C.   +10 more
europepmc   +1 more source