Zobrazeno 1 - 10
of 527
pro vyhledávání: '"osteochondromas"'
Autor:
Tadamasa Handa, Kunihiro Asanuma, Hiroto Yuasa, Tomoki Nakamura, Tomohito Hagi, Katsunori Uchida, Akihiro Sudo
Publikováno v:
Case Reports in Oncology, Vol 17, Iss 1, Pp 1266-1272 (2024)
Introduction: Osteochondromas are benign tumors that arise primarily in the metaphyseal region of long bones. The malignant transformation rate is estimated to be less than 1% and 1–3% in solitary and multiple osteochondromas, respectively. Transfo
Externí odkaz:
https://doaj.org/article/53a48caf26f745f0a3b3c62899e027ed
Publikováno v:
Journal of Current Ophthalmology, Vol 35, Iss 4, Pp 411-414 (2024)
Purpose: To study rare ocular findings in a rare case of hereditary multiple exostoses (HME) and to study HME in one family. Methods: HME is an autosomal dominant genetic disease characterized by the presence of multiple exostoses (osteochondromas).
Externí odkaz:
https://doaj.org/article/e29c990dfa64410595ff795a72c87965
Autor:
Federica Masino, MD, Manuela Montatore, MD, Rossella Carpentiere, MD, Marina Balbino, MD, Rossella Gifuni, MD, Giacomo Fascia, MD, Giuseppe Guglielmi, MD
Publikováno v:
Radiology Case Reports, Vol 19, Iss 8, Pp 2943-2949 (2024)
We present a case of hereditary multiple exostoses with malignant transformation to chondrosarcoma in a woman complaining of enlargement and pain in the right thigh. Hereditary multiple exostoses is a rare genetic disorder characterized by multiple o
Externí odkaz:
https://doaj.org/article/a850b0cc57c245beb88e77c376b49d67
Autor:
Longqing Li, Minxun Lu, Xuanhong He, Chang Zou, Chuanxi Zheng, Yitian Wang, Fan Tang, Yi Luo, Yong Zhou, Li Min, Chongqi Tu
Publikováno v:
Orthopaedic Surgery, Vol 16, Iss 3, Pp 781-787 (2024)
Background Fibrodysplasia ossificans progressiva (FOP) is an extremely rare disease characterized by malformation of the bilateral great toes and progressive heterotopic ossification. The clinical features of FOP occur due to dysfunction of the bone
Externí odkaz:
https://doaj.org/article/9cf2ffd27bf7421d9d10559c3c421e9d
Autor:
Artem Borovikov, Andrey Marakhonov, Aysylu Murtazina, Kseniya Davydenko, Alexandra Filatova, Nailya Galeeva, Varvara Kadnikova, Natalya Ogorodova, Daria Gorodilova, Ilya Kanivets, Denis Pyankov, Konstantin Zherdev, Aleksandr Petel’guzov, Pavel Zubkov, Alexander Polyakov, Olga Shchagina, Mikhail Skoblov
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Multiple osteochondromas (MO) is a rare autosomal dominant skeletal disorder characterized by the development of multiple benign tumors known as osteochondromas. The condition is predominantly caused by loss-of-function variants in the EXT1 or EXT2 g
Externí odkaz:
https://doaj.org/article/9b18c72810344e36991efc0b72f3c6ef
Autor:
Maria Gnoli, Marco Gambarotti, Alberto Righi, Eric Lodewijk Staals, Andrea Evangelista, Morena Tremosini, Evelise Brizola, Marina Mordenti, Manila Boarini, Manuela Locatelli, Elena Pedrini, Luca Sangiorgi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Multiple osteochondromas is genetic disorder characterized by the formation of multiple benign cartilage-capped bone tumors, named osteochondromas, during skeletal development. The most feared complication is the secondary periphe
Externí odkaz:
https://doaj.org/article/39630631ea254982b0c1ea691e0ae7c2
Autor:
Valeria Calogero, Michela Florio, Silvia Careri, Angelo Gabriele Aulisa, Francesco Falciglia, Marco Giordano
Publikováno v:
Diseases, Vol 12, Iss 8, p 167 (2024)
Background: Heel pain in children is a common condition. The aetiology can be ascribed to fractures, osteochondrosis, tendinitis, calcaneal-navicular or talo-calcaneal coalition, osteomyelitis, rheumatic diseases, anatomic variants, malignant tumours
Externí odkaz:
https://doaj.org/article/70cb6118a0c643739c97990671dded04
Publikováno v:
Clinical Case Reports, Vol 11, Iss 8, Pp n/a-n/a (2023)
Key Clinical Message Osteochondromas (OCs) are developmental anomalies that originate from the periosteum and typically form during enchondral ossification near the joints. Retro‐patellar OC caused by exostosis forms in various intracapsular, intra
Externí odkaz:
https://doaj.org/article/e416b4b202db4811b131e7bd3d90762c
Akademický článek
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Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
ObjectiveTo investigate the effect of modified gradual ulnar lengthening in the treatment of Masada type IIb forearm deformity in children with hereditary multiple osteochondromas (HMO).Patients and methodsFrom May 2015 to October 2020, 12 children w
Externí odkaz:
https://doaj.org/article/a9e0c414cc364b308575d867c2fec69c