Literature DB >> 23853506

An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member.

Francesca Trojsi1, Giovanni Piccirillo, Cinzia Femiano, Raffaele Damiano, Maria Rosaria Monsurrò.   

Abstract

We report the first Italian kindred with Familial Amyotrophic Lateral Sclerosis (FALS) due to c.149T>C mutation in the exon 5 of superoxide dismutase-1 (SOD1) gene. The proband was a 49-year-old woman who came to our observation because of an history of progressive limbs weakness and gait impairment. She belonged to a family of 24 affected members. The prevalent phenotype of the affected members was characterized by slowly progressive spinal impairment with proximal distribution of weakness, and bulbar involvement in advanced stages. We briefly reviewed the few previous reports about the same SOD1 mutation and discussed the hypothesis that structural instability of the mutant codon 149 protein may underlie some toxic effects significantly involved in FALS pathogenesis.

Entities:  

Keywords:  Familial ALS (FALS); mutation; superoxide dismutase 1 (SOD1)

Mesh:

Substances:

Year:  2013        PMID: 23853506      PMCID: PMC3665374     

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


  10 in total

Review 1.  El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis.

Authors:  B R Brooks; R G Miller; M Swash; T L Munsat
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2.  SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.

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Journal:  J Med Genet       Date:  2010-06-24       Impact factor: 6.318

3.  Two novel mutations in the gene for copper zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis.

Authors:  Z E Enayat; R W Orrell; A Claus; A Ludolph; R Bachus; J Brockmüller; K Ray-Chaudhuri; A Radunovic; C Shaw; J Wilkinson
Journal:  Hum Mol Genet       Date:  1995-07       Impact factor: 6.150

4.  Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutation.

Authors:  Gardian C Y Fong; Ken H H Kwok; Y Q Song; T S Cheng; Philip W L Ho; Andrew C Y Chu; Michelle H W Kung; K H Chan; Windsor Mak; Raymond T F Cheung; David B Ramsden; S L Ho
Journal:  Amyotroph Lateral Scler       Date:  2006-09

5.  SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.

Authors:  Stefania Battistini; Fabio Giannini; Giuseppe Greco; Giuseppe Bibbò; Loreta Ferrera; Valeria Marini; Renzo Causarano; Michela Casula; Giuliana Lando; Maria Cristina Patrosso; Claudia Caponnetto; Paola Origone; Alessandro Marocchi; Alberto Del Corona; Gabriele Siciliano; Paola Carrera; Vincenzo Mascia; Marcello Giagheddu; Carlo Carcassi; Sandro Orrù; Cecilia Garrè; Silvana Penco
Journal:  J Neurol       Date:  2005-03-29       Impact factor: 4.849

6.  Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.

Authors:  A Pramatarova; D A Figlewicz; A Krizus; F Y Han; I Ceballos-Picot; A Nicole; M Dib; V Meininger; R H Brown; G A Rouleau
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

7.  A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.

Authors:  Alan E Renton; Elisa Majounie; Adrian Waite; Javier Simón-Sánchez; Sara Rollinson; J Raphael Gibbs; Jennifer C Schymick; Hannu Laaksovirta; John C van Swieten; Liisa Myllykangas; Hannu Kalimo; Anders Paetau; Yevgeniya Abramzon; Anne M Remes; Alice Kaganovich; Sonja W Scholz; Jamie Duckworth; Jinhui Ding; Daniel W Harmer; Dena G Hernandez; Janel O Johnson; Kin Mok; Mina Ryten; Danyah Trabzuni; Rita J Guerreiro; Richard W Orrell; James Neal; Alex Murray; Justin Pearson; Iris E Jansen; David Sondervan; Harro Seelaar; Derek Blake; Kate Young; Nicola Halliwell; Janis Bennion Callister; Greg Toulson; Anna Richardson; Alex Gerhard; Julie Snowden; David Mann; David Neary; Michael A Nalls; Terhi Peuralinna; Lilja Jansson; Veli-Matti Isoviita; Anna-Lotta Kaivorinne; Maarit Hölttä-Vuori; Elina Ikonen; Raimo Sulkava; Michael Benatar; Joanne Wuu; Adriano Chiò; Gabriella Restagno; Giuseppe Borghero; Mario Sabatelli; David Heckerman; Ekaterina Rogaeva; Lorne Zinman; Jeffrey D Rothstein; Michael Sendtner; Carsten Drepper; Evan E Eichler; Can Alkan; Ziedulla Abdullaev; Svetlana D Pack; Amalia Dutra; Evgenia Pak; John Hardy; Andrew Singleton; Nigel M Williams; Peter Heutink; Stuart Pickering-Brown; Huw R Morris; Pentti J Tienari; Bryan J Traynor
Journal:  Neuron       Date:  2011-09-21       Impact factor: 17.173

Review 8.  The microglial-motoneuron dialogue in ALS.

Authors:  S H Appel; W Zhao; D R Beers; J S Henkel
Journal:  Acta Myol       Date:  2011-06

Review 9.  Familial amyotrophic lateral sclerosis, a historical perspective.

Authors:  T Siddique; S Ajroud-Driss
Journal:  Acta Myol       Date:  2011-10

10.  TARDBP mutations are not a frequent cause of ALS in Finnish patients.

Authors:  Hanna-Kaisa Mentula; Laura Tuovinen; Sini Penttilä; Tiina Suominen; Bjarne Udd; Johanna Palmio
Journal:  Acta Myol       Date:  2012-10
  10 in total
  1 in total

1.  A novel splice-site mutation in ALS2 establishes the diagnosis of juvenile amyotrophic lateral sclerosis in a family with early onset anarthria and generalized dystonias.

Authors:  Saima Siddiqi; Jia Nee Foo; Anthony Vu; Saad Azim; David L Silver; Atika Mansoor; Stacey Kiat Hong Tay; Sumiya Abbasi; Asraf Hussain Hashmi; Jamal Janjua; Sumbal Khalid; E Shyong Tai; Gene W Yeo; Chiea Chuen Khor
Journal:  PLoS One       Date:  2014-12-04       Impact factor: 3.240

  1 in total

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