Melorheostosis in a Pediatric Patient

2005 ◽  
Vol 95 (2) ◽  
pp. 167-170 ◽  
Author(s):  
Michael A. Schreck

Melorheostosis is a nonhereditary and uncommon condition that can affect both adults and children. It can appear on radiographs as increased sclerosis on bones of the upper and lower extremities and may mimic other bony conditions such as osteopoikilosis, osteopetrosis, arthrogryposis multiplex congenita, and osteopathia striata. The sclerotic appearance can differ greatly between adults and children. The skin and subcutaneous tissues may be affected by fibrosis, resulting in contractures of joints and limbs that lead to deformities and limb-length discrepancies. This article reviews the literature on melorheostosis and describes a case in a 10-year-old boy. (J Am Podiatr Med Assoc 95(2): 167–170, 2005)

2016 ◽  
Vol 71 (3) ◽  
pp. 372-376 ◽  
Author(s):  
L Otten ◽  
A Bosy-Westphal ◽  
J Ordemann ◽  
E Rothkegel ◽  
N Stobäus ◽  
...  

Author(s):  
Cody R. Perskin ◽  
Abhijit Seetharam ◽  
Brian H. Mullis ◽  
Andrew J. Marcantonio ◽  
John Garfi ◽  
...  

1994 ◽  
Vol 37 (2) ◽  
pp. 230-236 ◽  
Author(s):  
Kazuhiko Yokoyama ◽  
Masateru Shindo ◽  
Moritoshi Itoman ◽  
Makoto Yamamoto

1935 ◽  
Vol 31 (8-9) ◽  
pp. 1012-1017
Author(s):  
G. M. Novikov

In 1862, Raynaud first described, as a completely independent nosological unit, a kind of disease of the peripheral and most protruding parts of the body (fingers of the upper and lower extremities, auricles, the tip of the nose, cheeks), now known under the name of Raynaud's symmetric gangrene ... Since that time, little new has been introduced into the etiology and pathogenesis of this disease.


2007 ◽  
Vol 25 (11) ◽  
pp. 3476-3487 ◽  
Author(s):  
Eiichi Naito ◽  
Tokuro Nakashima ◽  
Tomonori Kito ◽  
Yu Aramaki ◽  
Tomohisa Okada ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document