Literature DB >> 19435728

Severe neuropathy after diphtheria-tetanus-pertussis vaccination in a child carrying a novel frame-shift mutation in the small heat-shock protein 27 gene.

Paola Mandich1, Marina Grandis, Alessandra Varese, Alessandro Geroldi, Massimo Acquaviva, Paola Ciotti, Rossella Gulli, Laura Doria-Lamba, Gian Maria Fabrizi, Gaia Giribaldi, Antonio Pizzuti, Angelo Schenone, Emilia Bellone.   

Abstract

Mutations in small heat-shock protein 27 and small heat-shock protein 22 genes were found in association with Charcot-Marie-Tooth disease type 2 and distal hereditary motor neuropathy. We searched for mutations in small heat-shock protein 27 gene in an Italian family with peripheral neuropathy and intrafamilial phenotypic variability. A novel heterozygous frame-shift mutation c.476_477delCT was found while point mutations in most genes associated with hereditary neuropathies were ruled out. In the proband, who showed a severe early onset peripheral neuropathy, an independent pathogenetic effect on the peripheral nervous system secondary to the tetanus toxoid injection may be supposed. This is the first truncating nonsense mutation in the small heat-shock protein 27 gene identified so far and the clinical, neurophysiologic, and neuropathological findings are discussed.

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Year:  2009        PMID: 19435728     DOI: 10.1177/0883073809334387

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  9 in total

Review 1.  Neuropathy- and myopathy-associated mutations in human small heat shock proteins: Characteristics and evolutionary history of the mutation sites.

Authors:  Rainer Benndorf; Jody L Martin; Sergei L Kosakovsky Pond; Joel O Wertheim
Journal:  Mutat Res Rev Mutat Res       Date:  2014-03-06       Impact factor: 5.657

2.  Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family.

Authors:  Claudia Stancanelli; Gian Maria Fabrizi; Moreno Ferrarini; Tiziana Cavallaro; Federica Taioli; Rita Di Leo; Massimo Russo; Luca Gentile; Antonio Toscano; Giuseppe Vita; Anna Mazzeo
Journal:  Neurol Sci       Date:  2014-12-30       Impact factor: 3.307

Review 3.  The Genetics of Spinal Muscular Atrophy: Progress and Challenges.

Authors:  Michelle A Farrar; Matthew C Kiernan
Journal:  Neurotherapeutics       Date:  2015-04       Impact factor: 7.620

Review 4.  Mutations in HspB1 and hereditary neuropathies.

Authors:  Lydia K Muranova; Maria V Sudnitsyna; Sergei V Strelkov; Nikolai B Gusev
Journal:  Cell Stress Chaperones       Date:  2020-04-16       Impact factor: 3.667

Review 5.  Molecular chaperones and neuronal proteostasis.

Authors:  Heather L Smith; Wenwen Li; Michael E Cheetham
Journal:  Semin Cell Dev Biol       Date:  2015-03-12       Impact factor: 7.727

Review 6.  Chaperonopathies: Spotlight on Hereditary Motor Neuropathies.

Authors:  Vincenzo Lupo; Carmen Aguado; Erwin Knecht; Carmen Espinós
Journal:  Front Mol Biosci       Date:  2016-12-14

Review 7.  Small heat shock proteins in neurodegenerative diseases.

Authors:  Leen Vendredy; Elias Adriaenssens; Vincent Timmerman
Journal:  Cell Stress Chaperones       Date:  2020-04-22       Impact factor: 3.667

8.  Charcot-Marie-Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments.

Authors:  Anne Holmgren; Delphine Bouhy; Vicky De Winter; Bob Asselbergh; Jean-Pierre Timmermans; Joy Irobi; Vincent Timmerman
Journal:  Acta Neuropathol       Date:  2013-06-01       Impact factor: 17.088

9.  Truncated HSPB1 causes axonal neuropathy and impairs tolerance to unfolded protein stress.

Authors:  Emil Ylikallio; Svetlana Konovalova; Yogesh Dhungana; Taru Hilander; Nella Junna; Juhani V Partanen; Jussi P Toppila; Mari Auranen; Henna Tyynismaa
Journal:  BBA Clin       Date:  2015-03-11
  9 in total

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