Radiological features of Paget disease of bone associated with VCP myopathy

Objective Mutations 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 si...

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Veröffentlicht in:	Skeletal radiology 2012-03, Vol.41 (3), p.329-337
Hauptverfasser:	Farpour, Farzin, Tehranzadeh, Jamshid, Donkervoort, Sandra, Smith, Charles, Martin, Barbara, Vanjara, Pari, Osann, Kathryn, Kimonis, Virginia E.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adenosine Triphosphatases - genetics Adult Age Aged Alkaline phosphatase Bisphosphonates Bone diseases Cell Cycle Proteins - genetics Comparative analysis Dementia Female Frontotemporal dementia Humans Imaging Inclusion bodies Male Medical colleges Medicine Medicine & Public Health Mutation Myopathy Myositis, Inclusion Body - diagnostic imaging Myositis, Inclusion Body - genetics Nuclear Medicine Orthopedics Osteitis Deformans - diagnostic imaging Osteitis Deformans - genetics Pathology Phosphatases Radiography Radiology Scientific Article Surveys Valosin Containing Protein
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