Late-onset Huntington disease with intermediate CAG repeats: true or false?

Justus L. Groen, Rob M. A. de Bie, Elisabeth M. J. Foncke, Raymund A. C. Roos, Klaus L. Leenders, Marina A. J. Tijssen*

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    48 Citations (Scopus)

    Abstract

    Huntington disease (HD) is a neurodegenerative disorder associated with an expanded CAG trinucleotide repeat length in the huntingtin gene. 'Intermediate alleles' with 27 to 35 CAG repeats generally do not cause HD but are unstable upon germ-line transmission. Insights in CAG repeat mosaicism and enhanced trinucleotide expansion in postmitotic neurons indicate that in the intermediate range, other factors than the CAG repeat length in diagnostic tests have to be considered. Here, we report two patients with mild, late onset HD and an intermediate repeat allele. The authors anticipate that intermediate repeats can cause late-onset HD due to disease modifiers and may be more common than previously stated.

    Original languageEnglish
    Pages (from-to)228-230
    Number of pages3
    JournalJOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    Volume81
    Issue number2
    DOIs
    Publication statusPublished - Feb-2010

    Keywords

    • 29 TRINUCLEOTIDE REPEATS
    • AGE-OF-ONSET
    • INSTABILITY
    • EXPANSION
    • PHENOCOPIES
    • ALLELES
    • RE

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