rare bone disease
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2021 ◽  
Vol 11 ◽  
Author(s):  
Peter Kloen ◽  
Reggie Charles Hamdy ◽  
Niels Hendrik Bech

IntroductionInjuries to the quadriceps extensor mechanism are rare in patients with Osteogenesis Imperfecta (OI). To the best of our knowledge, non-union of the patella in OI, either as an isolated problem or in combination with an acute fracture, has not been previously reported.Case reportWe describe how we surgically approached both the fracture and the non-union simultaneously. The surgical technique and steps are described in detail. Post-operative course was uneventful and the outcome was favorable, with full return of function for the patient.ConclusionA review of various knee extensor mechanism injuries in OI is described as illustrated in a single patient. The unusual simultaneous surgical treatment of a non-union and an acute fracture in the same patella shows that despite the severely compromised bone in this rare bone disease the bone still has a capacity to heal with a functional outcome.


2020 ◽  
Vol 18 (4) ◽  
pp. 344-349
Author(s):  
Laura L. Tosi ◽  
Elmer N. Rajah ◽  
Michael H. Stewart ◽  
Austin P. Gillies ◽  
Tracy S. Hart ◽  
...  

2018 ◽  
Vol 30 (2) ◽  
pp. 507-511 ◽  
Author(s):  
T. Swezey ◽  
B.B. Reeve ◽  
T.S. Hart ◽  
M.K. Floor ◽  
C.M. Dollar ◽  
...  

Author(s):  
M I Muzykin ◽  
A K Iordanishvili ◽  
M G Rybakova ◽  
V N Bugera ◽  
S V Vasiliev

This article presents the results of the clinical examination of the patient at the age of 41, who has been hospitalized according to the principle of OMC to the department of oral surgery and multi- specialized hospital of stomatology with a rare bone disease which affects the lower jaw -desmoplastic fibroma. The surveillance has been conducted for three years. Clinical characteristics and Хray patterns of the disease were revealed and the results of instrumental and histological studies were shown.


2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
Nilufer Ozdemir Kutbay ◽  
Banu Sarer Yurekli ◽  
Emine Kartal Baykan ◽  
Serap Baydur Sahin ◽  
Fusun Saygili

Aim. Fibrous dysplasia is a rare bone disease caused by missense mutation leading to abnormal fibroblast and osteoblast proliferation and increased bone resorption. FD can present in monostotic or polyostotic forms. About 3% of FD could be in association with McCune-Albright syndrome (MAS). Because FD is a rare disease, there is limited data in the literature about characteristics of disease and response to treatment.Methods. We present our five cases of FD with general properties and their responses to medical treatment.Results. Two of our patients had polyostotic and three had monostotic FD. One of the polyostotic patients had MAS. One of our patients had surgery for femur fractures, facial asymmetry, and findings of compression. Four patients were given pamidronate; one was given zoledronic acid as bisphosphonate treatment. Bone pain was relieved in all patients with medical treatment.Conclusion. There was a decrease in bone turnover markers to some degree with medical treatment but no radiological improvement was observed.


Bone Research ◽  
2013 ◽  
Vol 1 (4) ◽  
pp. 301-310 ◽  
Author(s):  
Charles R. Farber ◽  
Thomas L. Clemens

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