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Radiological features of Paget disease of bone associated with VCP myopathy |
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| Authors: | Farzin?Farpour,Jamshid?Tehranzadeh,Sandra?Donkervoort,Charles?Smith,Barbara?Martin,Pari?Vanjara,Kathryn?Osann,Virginia?E.?Kimonis mailto:vkimonis@uci.edu" title=" vkimonis@uci.edu" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author |
| Affiliation: | (1) Department of Radiology, VA Long Beach Health Care, University of California, Irvine, CA, USA;(2) Division of Genetics and Metabolism, Department of Pediatrics, University of California, Irvine, CA, USA;(3) Present address: Mount Sinai School of Medicine, Queens Hospital Center, New York, NY, USA;(4) Department of Neurology and Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY, USA;(5) University of Kentucky, Lexington, KY, USA;(6) Department of Medicine, Division of Hematology/Oncology, University of California, Irvine, CA, USA;(7) Division of Genetics and Metabolism, UC Irvine Medical Center, 101 The City Drive South, ZC 4482, Orange, CA 92868, USA |
| Abstract: | ObjectiveMutations in the Valosin-containing protein (VCP) gene cause a unique disorder characterized by classic Paget disease of bone (PDB), inclusion body myopathy, and frontotemporal dementia (IBMPFD). Our objective was to analyze the radiographic features of PDB associated with VCP mutations since there is a dearth of literature on the PDB component of VCP disease. |
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