Special Feature

User Panel

My Panel

My Panel

Bookmark Science Articles

Recent News
Bookmark / Share This Science Site

FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening.

FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

  • Abstract Text of This Paper
  • Journal Published
  • MeSH Keywords of This Abstract
  • Chemicals and Substances Used in this Paper
  • Grants and Granting Agency of this Research
  • Database Accession Numbers Used in this Paper
  • Related Papers
  • Related Research Tags
  • Rate this Research Paper
  • FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening. Abstract Text:

    laia rodriguez-revengaLaia Rodriguez-Revenga,beatriz Beatriz ,esteban Esteban ,dolores Dolores ,monica santosMonica Santos,mar Mar ,gisela Gisela ,luis brievaLuis Brieva,montserrat Montserrat ,laia rodriguez-revengaLaia Rodriguez-Revenga,beatriz Beatriz ,esteban Esteban ,dolores Dolores ,monica santosMonica Santos,mar Mar ,gisela Gisela ,luis brievaLuis Brieva,montserrat Montserrat ,

    Fragile X-associated tremor/ataxia syndrome (FXTAS) is a newly described disorder characterized by progressive action tremor and ataxia that occurs in premutation carriers of the FMR1 gene. The incidence of FMR1 premutated carriers in the general population is relatively high, and therefore FXTAS might explain a considerable number of sporadic, late-onset ataxias. To better establish the prevalence of FXTAS among undiagnosed Spanish patients with ataxia, we have performed a FMR1 premutation screening. Our results evidenced three individuals carrying premutated alleles, giving an estimated FXTAS prevalence of 1.95% among patients with late-onset ataxia (1.15% for males and 3% for females). Molecular characterization of premutation carriers evidences lower fragile X mental retardation 1 protein levels and increased FMR1 mRNA levels. Clinical and neuroimaging findings support FXTAS diagnosis in these patients. Because of the high prevalence of FMR1 premutation in the general population, the description and characterization of the FXTAS syndrome is of great interest as it may represent one of the more common monogenic causes of ataxia, tremor, and dementia. The results obtained in this study demonstrate that FXTAS should be incorporated to spinocerebellar ataxia genetic screening protocols. Early diagnosis of these patients benefits not only them but also the rest of the family that should be advised for the fragile X syndrome.

    FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening. Publishing Authors By Initials

    l rodriguez-revengaL Rodriguez-Revenga,b B ,e E ,d D ,m santosM Santos,m M ,g G ,l brievaL Brieva,m M ,l rodriguez-revengaL Rodriguez-Revenga,b B ,e E ,d D ,m santosM Santos,m M ,g G ,l brievaL Brieva,m M ,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Molecular neurobiology

    VOLUME: 35

    Page Numbers: 324-8

    Journal Abbreviation: Mol. Neurobiol.

    ISSN: 0893-7648

    DAY: 5

    MONTH: Jun

    YEAR: 2007

    FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8900963

    FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening. Keywords Mesh Terms:

    KEYWORDS:

    MESH TERMS:

    Chemical & Substance for Abstract: FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening. Information

    Substance Name:

    Registry Number:

    Grant and Affiliation Information for FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening.

    AFFILIATION: Biochemistry and Molecular Genetics Department, Hospital Clínic, Barcelona, Spain.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY:

    GRANT:

    ACRONYM:

    MEDLINETA: Mol Neurobiol

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

    FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening Related Publications

     

    Molecular Station USER Menu

    Welcome to Molecular Station!

    You have to register before you can post on our forums or use our advanced features. Register Now! Its Free and Fast!

    Already registered? Login now below.

    User Name:

    Password:

    Already registered and Forgot your password? Click below to recover it.

    Recover Lost Password

    Join now - it's fast and free!

    Molecular Station is THE largest network of researchers, scientists and science lovers anywhere!

    Research Terms of Usage and Disclaimer
    Home
    Features

    Protocols

    DNA Forum

    Science Forum

    DNA Forum
    Biology Forum

    Science News


    [CaRP] XML error: Invalid document end at line 2

    For more click here:Science News