Camurati‐Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment

Camurati‐Engelmann disease (CED) is a rare autosomal dominant type of bone dysplasia. This review is based on the unpublished and detailed clinical, radiological, and molecular findings in 14 CED families, comprising 41 patients, combined with data from 10 other previously reported CED families. For...

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Bibliografski detalji
Glavni autori: Janssens, K, Vanhoenacker, F, Bonduelle, M, Verbruggen, L, Van Maldergem, L, Ralston, S, Guañabens, N, Migone, N, Wientroub, S, Divizia, M T, Bergmann, C, Bennett, C, Simsek, S, Melançon, S, Cundy, T, Van Hul, W
Format: Artigo
Jezik:Inglês
Izdano: BMJ Group 2006
Teme:
Review
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2564495/
https://ncbi.nlm.nih.gov/pubmed/15894597
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.033522
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