Literature DB >> 20128141

Unusual association of FSHD and extramedullary thoracic tumour in the same patient: a case report.

V Kazakov1, D Rudenko, J Schulev, A Pozdnyakov.   

Abstract

In the recent literature the association of facioscapulohumeral-dystrophy (FSHD) with some hereditary neuromuscular diseases in the same patient has been reported. We present the first case in which the genetically confirmed familial FSHD is associated with an extramedullary thoracic tumour.

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Mesh：

Year:  2009        PMID： 20128141      PMCID： PMC2858950     

Source DB:  PubMed          Journal:  Acta Myol        ISSN： 1128-2460


  8 in total

1.  Facioscapulohumeral muscular dystrophy and myasthenia gravis co-existing in the same patient: a case report.

Authors:  A McGonigal; A M Thomas; R K H Petty
Journal:  J Neurol       Date:  2002-02       Impact factor: 4.849

2.  An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy.

Authors:  W L Chuenkongkaew; P Lertrit; C Limwongse; Y Nilanont; K Boonyapisit; T Sangruchi; N Chirapapaisan; R Suphavilai
Journal:  Eur J Neurol       Date:  2005-05       Impact factor: 6.089

3.  Diagnostic challenges in facioscapulohumeral muscular dystrophy.

Authors:  S Sacconi; L Salviati; I Bourget; D Figarella; Y Péréon; R Lemmers; S van der Maarel; C Desnuelle
Journal:  Neurology       Date:  2006-10-24       Impact factor: 9.910

4.  The devastating combination of Charcot-Marie-Tooth disease and facioscapulohumeral muscular dystrophy.

Authors:  C M Bütefisch; D F Lang; L Gutmann
Journal:  Muscle Nerve       Date:  1998-06       Impact factor: 3.217

5.  Dysphagia in facioscapulohumeral muscular dystrophy.

Authors:  M Wohlgemuth; B J M de Swart; J G Kalf; F B M Joosten; A M Van der Vliet; G W Padberg
Journal:  Neurology       Date:  2006-06-27       Impact factor: 9.910

6.  Novel mitochondrial tRNA Leu(CUN) transition and D4Z4 partial deletion in a patient with a facioscapulohumeral phenotype.

Authors:  Massimiliano Filosto; Paola Tonin; Mauro Scarpelli; Chiara Savio; Francesca Greco; Michelangelo Mancuso; Gaetano Vattemi; Vittorio Govoni; Nicolò Rizzuto; Rossella Tupler; Giuliano Tomelleri
Journal:  Neuromuscul Disord       Date:  2008-03-14       Impact factor: 4.296

7.  Phenotype of combined Duchenne and facioscapulohumeral muscular dystrophy.

Authors:  Lawrence Korngut; Victoria M Siu; Shannon L Venance; Simon Levin; Peter Ray; Richard J L F Lemmers; Julia Keith; Craig Campbell
Journal:  Neuromuscul Disord       Date:  2008-06-30       Impact factor: 4.296

8.  Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype.

Authors:  S Rudnik-Schöneborn; J Weis; W Kress; M Häusler; K Zerres
Journal:  Neuromuscul Disord       Date:  2008-08-05       Impact factor: 4.296
  8 in total
  2 in total

1.  Facioscapulohumeral dystrophy myoblasts efficiently repair moderate levels of oxidative DNA damage.

Authors:  Yara Bou Saada; Carla Dib; Petr Dmitriev; Aline Hamade; Gilles Carnac; Dalila Laoudj-Chenivesse; Marc Lipinski; Yegor S Vassetzky
Journal:  Histochem Cell Biol       Date:  2016-02-09       Impact factor: 4.304

2.  Cancer-related genes in the transcription signature of facioscapulohumeral dystrophy myoblasts and myotubes.

Authors:  Petr Dmitriev; Ulykbek Kairov; Thomas Robert; Ana Barat; Vladimir Lazar; Gilles Carnac; Dalila Laoudj-Chenivesse; Yegor S Vassetzky
Journal:  J Cell Mol Med       Date:  2013-12-17       Impact factor: 5.310
  2 in total

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