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Volume 7 Supplement 1

International Meeting on Fibrous Dysplasia/McCune-Albright Syndrome and Cherubism

Proceedings

Edited by Michael T Collins

The International Meeting on Fibrous Dysplasia/McCune-Albright Syndrome and Cherubism: Best Clinical Practice and Future Research was funded by the Fibrous Dysplasia Foundation, and the National Institutes of Health (Division of Intramural Research National Institute of Dental and Craniofacial Research and Office of Rare Diseases). Publication of the proceedings was funded by the Fibrous Dysplasia Foundation and an unrestricted grant from Zimmer.

International Meeting on Fibrous Dysplasia/McCune-Albright Syndrome and Cherubism: Best Clinical Practice and Future Research.

Bethesda, MD, USA3-5 October 2010

  1. The surgical management of Polyostotic Fibrous Dysplasia (FD) of bone is technically demanding. The most effective methods to manage the associated bone deformity remain unclear. The marked variation in the de...

    Authors: Robert P Stanton, Ernesto Ippolito, Dempsey Springfield, Lynn Lindaman, Shlomo Wientroub and Arabella Leet
    Citation: Orphanet Journal of Rare Diseases 2012 7(Suppl 1):S1
  2. Fibrous dysplasia (FD) is a non-malignant condition caused by post-zygotic, activating mutations of the GNAS gene that results in inhibition of the differentiation and proliferation of bone-forming stromal cells ...

    Authors: JS Lee, EJ FitzGibbon, YR Chen, HJ Kim, LR Lustig, SO Akintoye, MT Collins and LB Kaban
    Citation: Orphanet Journal of Rare Diseases 2012 7(Suppl 1):S2
  3. One of the most common complications of fibrous dysplasia of bone (FD) is bone pain. Usual pain killers are often of inadequate efficacy to control this bone pain. The mechanism of bone pain in FD remains unce...

    Authors: Roland D Chapurlat, Deborah Gensburger, Juan M Jimenez-Andrade, Joseph R Ghilardi, Marilyn Kelly and Patrick Mantyh
    Citation: Orphanet Journal of Rare Diseases 2012 7(Suppl 1):S3
  4. Fibrous dysplasia (FD) is sometimes accompanied by extraskeletal manifestations that can include any combination of café-au-lait macules, hyperfunctioning endocrinopathies, such as gonadotropin-independent pre...

    Authors: Michael T Collins, Frederick R Singer and Erica Eugster
    Citation: Orphanet Journal of Rare Diseases 2012 7(Suppl 1):S4
  5. Cherubism is a rare bone dysplasia that is characterized by symmetrical bone resorption limited to the jaws. Bone lesions are filled with soft fibrous giant cell-rich tissue that can expand and cause severe fa...

    Authors: Ernst J Reichenberger, Michael A Levine, Bjorn R Olsen, Maria E Papadaki and Steven A Lietman
    Citation: Orphanet Journal of Rare Diseases 2012 7(Suppl 1):S5
  6. Cherubism is a skeletal dysplasia characterized by bilateral and symmetric fibro-osseous lesions limited to the mandible and maxilla. In most patients, cherubism is due to dominant mutations in the SH3BP2 gene on...

    Authors: Maria E Papadaki, Steven A Lietman, Michael A Levine, Bjorn R Olsen, Leonard B Kaban and Ernst J Reichenberger
    Citation: Orphanet Journal of Rare Diseases 2012 7(Suppl 1):S6