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Intergeneration CAG expansion and contraction in a Chinese HD family

  • Yanping Tang
  • , Ying Wang
  • , Ping Yang
  • , Yuan Liu
  • , Bo Wang
  • , Robert Podolsky
  • , Richard McIndoe
  • , Cong Yi Wang*
  • *Corresponding author for this work
  • Huazhong University of Science and Technology
  • Augusta University
  • Department of Cell Biology and Genetics
  • Center for Biotechnology and Genomic Medicine

Research output: Contribution to journalArticlepeer-review

Abstract

The prevalence of juvenile-onset Huntington's disease (HD) is about ten times lower than adult HD. Here we report a Chinese HD family showing both intergeneration CAG expansion and contraction. The expansion resulted from a paternal transmission which leads to juvenile-onset HD for a 17-year-old Chinese boy (III-5). More interestingly, a contraction was noticed in a maternal transmission (III-3), which changed the CAG repeat from an expanded, disease-causing allele (48 repeats) to a normal or intermediate allele (34 repeats). Of note, the contraction resulted in a deletion of 14 CAG repeats, which is much larger than previously reported contractions. Our results are consistent with previous observations in Western Caucasians that juvenile-onset HD is more likely inherited through the male germline.

Original languageEnglish
Pages (from-to)242-244
Number of pages3
JournalAmerican Journal of Medical Genetics - Neuropsychiatric Genetics
Volume141 B
Issue number3
DOIs
Publication statusPublished - 5 Apr 2006
Externally publishedYes

Keywords

  • Contraction
  • Expansion
  • Germline
  • Huntington's disease (HD)
  • Single nucleotide polymorphism (SNP)
  • Trinucleotide

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