Literature DB >> 23263837

[Myofibrillary myopathy due to the ZASP mutation Ala147Thr : two cases with exclusively distal leg involvement].

T Kraya1, W Kress, D Stoevesant, M Deschauer, S Zierz.   

Abstract

This article describes two patients with late onset myofibrillary myopathy due the ZASP mutation Ala147Thr. The Z-band alternatively spliced PDZ motif containing protein (ZASP) is a sarcomeric protein and interacts with α-actinin at the Z-disk. So far, myopathy due the ZASP mutation Ala147Thr was usually associated with distal and proximal involvement. The two patients with the ZASP mutation Ala147Thr described here showed only distal involvement of the legs without proximal weakness and involvement of the upper limb 6 and 19 years after onset of muscle weakness, respectively.

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Year:  2013        PMID: 23263837     DOI: 10.1007/s00115-012-3689-0

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  10 in total

1.  Solution structure of ZASP PDZ domain; implications for sarcomere ultrastructure and enigma family redundancy.

Authors:  Yunghan Au; R Andrew Atkinson; Remo Guerrini; Geoff Kelly; Catherine Joseph; Steven R Martin; Frederick W Muskett; Alberto Pallavicini; Georgine Faulkner; Annalisa Pastore
Journal:  Structure       Date:  2004-04       Impact factor: 5.006

2.  Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy.

Authors:  Montse Olivé; Zagaa Odgerel; Amaia Martínez; Juan José Poza; Federico García Bragado; Ramón J Zabalza; Ivonne Jericó; Laura Gonzalez-Mera; Alexey Shatunov; Hee Suk Lee; Judith Armstrong; Elías Maraví; Maria Ramos Arroyo; Jordi Pascual-Calvet; Carmen Navarro; Carmen Paradas; Mariano Huerta; Fabian Marquez; Eduardo Gutierrez- Rivas; Adolf Pou; Isidre Ferrer; Lev G Goldfarb
Journal:  Neuromuscul Disord       Date:  2011-06-14       Impact factor: 4.296

3.  Late onset hereditary distal myopathy.

Authors:  W R Markesbery; R C Griggs; R P Leach; L W Lapham
Journal:  Neurology       Date:  1974-02       Impact factor: 9.910

Review 4.  Molecular biology of distal muscular dystrophies--sarcomeric proteins on top.

Authors:  Bjarne Udd
Journal:  Biochim Biophys Acta       Date:  2006-08-18

5.  Mutations in ZASP define a novel form of muscular dystrophy in humans.

Authors:  Duygu Selcen; Andrew G Engel
Journal:  Ann Neurol       Date:  2005-02       Impact factor: 10.422

Review 6.  Distal myopathies--new genetic entities expand diagnostic challenge.

Authors:  Bjarne Udd
Journal:  Neuromuscul Disord       Date:  2011-12-23       Impact factor: 4.296

Review 7.  Distal myopathies.

Authors:  B Udd; R Griggs
Journal:  Curr Opin Neurol       Date:  2001-10       Impact factor: 5.710

8.  Mutations in myotilin cause myofibrillar myopathy.

Authors:  Duygu Selcen; Andrew G Engel
Journal:  Neurology       Date:  2004-04-27       Impact factor: 9.910

9.  Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients.

Authors:  Duygu Selcen; Kinji Ohno; Andrew G Engel
Journal:  Brain       Date:  2004-01-07       Impact factor: 13.501

10.  Zaspopathy in a large classic late-onset distal myopathy family.

Authors:  R Griggs; A Vihola; P Hackman; K Talvinen; H Haravuori; G Faulkner; B Eymard; I Richard; D Selcen; A Engel; O Carpen; B Udd
Journal:  Brain       Date:  2007-03-02       Impact factor: 13.501

  10 in total
  1 in total

1.  Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies.

Authors:  Anna-Lena Semmler; Sabrina Sacconi; J Elisa Bach; Claus Liebe; Jan Bürmann; Rudolf A Kley; Andreas Ferbert; Roland Anderheiden; Peter Van den Bergh; Jean-Jacques Martin; Peter De Jonghe; Eva Neuen-Jacob; Oliver Müller; Marcus Deschauer; Markus Bergmann; J Michael Schröder; Matthias Vorgerd; Jörg B Schulz; Joachim Weis; Wolfram Kress; Kristl G Claeys
Journal:  Orphanet J Rare Dis       Date:  2014-08-01       Impact factor: 4.123

  1 in total

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