Literature DB >> 15390127

Parkinsonism, FXTAS, and FMR1 premutations.

Mathias Toft1, Jan Aasly, Gina Bisceglio, Charles H Adler, Ryan J Uitti, Anna Krygowska-Wajs, Timothy Lynch, Zbigniew K Wszolek, Matthew J Farrer.   

Abstract

The presence of late-onset neurological symptoms in male carriers of premutation expansions of the fragile X mental retardation 1 (FMR1) gene has been described recently. One of the clinical symptoms in this fragile X-associated tremor/ataxia syndrome (FXTAS) is parkinsonism. To test the possible association between expanded FMR1 alleles and Parkinson's disease (PD), we determined the size of the FMR1 CGG repeat in 414 male cases of clinically diagnosed parkinsonism, the majority of whom had PD. None of our patients had expanded FMR1 repeats within the premutation range (55-200 CGG repeats). Five patients (1.2%) carry intermediate-size alleles (41-54 CGG repeats). Expansions within the FMR1 gene are not associated with PD in our study. Copyright 2004 Movement Disorder Society.

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Year:  2005        PMID: 15390127     DOI: 10.1002/mds.20297

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  18 in total

1.  New clinical findings in the fragile X-associated tremor ataxia syndrome (FXTAS).

Authors:  Jorge L Juncos; Joash T Lazarus; Emily Graves-Allen; Lisa Shubeck; Michelle Rusin; Gloria Novak; Deborah Hamilton; Julia Rohr; Stephanie L Sherman
Journal:  Neurogenetics       Date:  2011-01-29       Impact factor: 2.660

2.  Identification of expanded alleles of the FMR1 gene among high-risk population in Indonesia by using blood spot screening.

Authors:  Tri Indah Winarni; Agustini Utari; Farmaditya E P Mundhofir; Tzuhan Tong; Blythe Durbin-Johnson; Sultana M H Faradz; Flora Tassone
Journal:  Genet Test Mol Biomarkers       Date:  2011-10-11

3.  Size bias of fragile X premutation alleles in late-onset movement disorders.

Authors:  Sebastien Jacquemont; Maureen A Leehey; Randi J Hagerman; Laurel A Beckett; Paul J Hagerman
Journal:  J Med Genet       Date:  2006-05-24       Impact factor: 6.318

Review 4.  FXTAS: a progressive neurologic syndrome associated with Fragile X premutation.

Authors:  Rob Willemsen; Edwin Mientjes; Ben A Oostra
Journal:  Curr Neurol Neurosci Rep       Date:  2005-09       Impact factor: 5.081

Review 5.  Advances in the genetics of Parkinson disease.

Authors:  Joanne Trinh; Matt Farrer
Journal:  Nat Rev Neurol       Date:  2013-07-16       Impact factor: 42.937

6.  A genetic study of the FMR1 gene in a Sardinian multiple sclerosis population.

Authors:  L Lorefice; S Tranquilli; G Fenu; M R Murru; J Frau; M Rolesu; G C Coghe; F Marrosu; M G Marrosu; E Cocco
Journal:  Neurol Sci       Date:  2015-07-21       Impact factor: 3.307

7.  Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism.

Authors:  Atefeh Entezari; Mahmoud Shekari Khaniani; Tayyeb Bahrami; Sima Mansoori Derakhshan; Hossein Darvish
Journal:  Neurol Sci       Date:  2016-10-01       Impact factor: 3.307

8.  Parkinsonism in FMR1 premutation carriers may be indistinguishable from Parkinson disease.

Authors:  Deborah A Hall; Katherine Howard; Randi Hagerman; Maureen A Leehey
Journal:  Parkinsonism Relat Disord       Date:  2008-06-20       Impact factor: 4.891

Review 9.  Unstable mutations in the FMR1 gene and the phenotypes.

Authors:  Danuta Loesch; Randi Hagerman
Journal:  Adv Exp Med Biol       Date:  2012       Impact factor: 2.622

10.  Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism.

Authors:  D Z Loesch; M S Khaniani; H R Slater; J P Rubio; Q M Bui; K Kotschet; W D'Souza; A Venn; P Kalitsis; A K H Choo; T Burgess; L Johnson; A Evans; M Horne
Journal:  Clin Genet       Date:  2009-09-30       Impact factor: 4.438

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