Literature DB >> 22699758

[Multilocular Paget's disease in IBMPFD syndrome. A case report with 14-year follow-up].

D Zajonz1, C Langsieb, L Chavdarova, S Kellermann, P Baum, C Wickenhauser, G von Salis-Soglio, T Prietzel.   

Abstract

Paget's osteodystrophia deformans is a monoostotic or polyostotic disease of the skeletal system with increased bone remodelling, structural modifications and skeletal deformation, typically arranged like a chessboard. The unusual case of a patient is described who had suffered from generalized Paget's disease of the bone for 14 years and also developed progressive myopathy and a behavioural variant frontotemporal dementia. Further cytogenetic diagnostics revealed a point mutation in the valosin-containing protein (VCP, p97) gene on chromosome 9p13-p12 consistent with the finding of inclusion body myopathy with early onset Paget's disease and frontotemporal dementia (IBMPFD syndrome). A causal therapy of this disease is not known. Conservative treatment with bisphosphonate therapy, intensive physiotherapeutic exercise and psychotherapeutic treatment was performed to retard the progression of the disease.

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Year:  2012        PMID: 22699758     DOI: 10.1007/s00132-012-1935-6

Source DB:  PubMed          Journal:  Orthopade        ISSN: 0085-4530            Impact factor:   1.087


  7 in total

Review 1.  Molecular diagnosis of facioscapulohumeral muscular dystrophy.

Authors:  Meena Upadhyaya; David N Cooper
Journal:  Expert Rev Mol Diagn       Date:  2002-03       Impact factor: 5.225

2.  Valosin-containing protein gene mutations: clinical and neuropathologic features.

Authors:  L Guyant-Maréchal; A Laquerrière; C Duyckaerts; C Dumanchin; J Bou; F Dugny; I Le Ber; T Frébourg; D Hannequin; D Campion
Journal:  Neurology       Date:  2006-06-21       Impact factor: 9.910

3.  Pathological consequences of VCP mutations on human striated muscle.

Authors:  Christian U Hübbers; Christoph S Clemen; Kristina Kesper; Annett Böddrich; Andreas Hofmann; Outi Kämäräinen; Karen Tolksdorf; Maria Stumpf; Julia Reichelt; Udo Roth; Sabine Krause; Giles Watts; Virginia Kimonis; Mike P Wattjes; Jens Reimann; Dietmar R Thal; Katharina Biermann; Bernd O Evert; Hanns Lochmüller; Erich E Wanker; Benedikt G H Schoser; Angelika A Noegel; Rolf Schröder
Journal:  Brain       Date:  2006-09-19       Impact factor: 13.501

4.  Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone.

Authors:  Nancy Laurin; Jacques P Brown; Jean Morissette; Vincent Raymond
Journal:  Am J Hum Genet       Date:  2002-04-30       Impact factor: 11.025

5.  Paget disease and sensorineural hearing loss associated with spiral ligament degeneration.

Authors:  Karen Borne Teufert; Fred Linthicum
Journal:  Otol Neurotol       Date:  2005-05       Impact factor: 2.311

Review 6.  Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia.

Authors:  Conrad C Weihl; Alan Pestronk; Virginia E Kimonis
Journal:  Neuromuscul Disord       Date:  2009-04-19       Impact factor: 4.296

7.  Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.

Authors:  Giles D J Watts; Jill Wymer; Margaret J Kovach; Sarju G Mehta; Steven Mumm; Daniel Darvish; Alan Pestronk; Michael P Whyte; Virginia E Kimonis
Journal:  Nat Genet       Date:  2004-03-21       Impact factor: 38.330

  7 in total

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