Skip Navigation


Rheumatology Advance Access originally published online on April 12, 2005
Rheumatology 2005 44(8):1069-1072; doi:10.1093/rheumatology/keh649
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
44/8/1069    most recent
keh649v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Ramanan, A. V.
Right arrow Articles by Mughal, Z.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ramanan, A. V.
Right arrow Articles by Mughal, Z.
Related Collections
Right arrow Rheumatoid Arthritis
Right arrow Osteoporosis and Osteopenia
Social Bookmarking
Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2005. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org

LETTER TO THE EDITOR

Camurati–Engelmann disease—a case report and literature review

A. V. Ramanan, M. J. Hall, E. M. Baildam and Z. Mughal1

Department of Paediatric Rheumatology, Royal Manchester Children's Hospital and 1 Department of Paediatrics, Saint Mary's Hospital, Manchester, UK

Correspondence to: A. V. Ramanan, Department of Paediatric Rheumatology, Southmead Hospital, Westbury-on-Trym, Bristol BS9 3SB, UK. E-mail: avramanan@hotmail.com

The first 10% of the full text of this article appears below.

SIR, Camurati–Engelmann disease is a rare autosomal dominant condition characterized by progressive diaphyseal dysplasia. We report a child presenting with non-specific limb pains and a waddling gait in whom the clinical and radiological appearances led to a diagnosis of Camurati-Engelmann disease.

A 4-yr-old boy presented with a history of pains in both lower limbs for ‘several years’, worsening over the preceding 3 months. The pain was localized to his calf and thigh muscles. The pain was initially only during the day but with time there was pain at night as well. He had . . . [Full Text of this Article]


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
 Rheumatology (Oxford)Home page
A. J. Taggart, S. A. Wright, E. Ball, D. Kane, and G. Wright
The Belfast musculoskeletal ultrasound course
Rheumatology, September 1, 2009; 48(9): 1073 - 1076.
[Abstract] [Full Text] [PDF]