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 language | English |
|---|---|
| Pages (from-to) | 242-244 |
| Number of pages | 3 |
| Journal | American Journal of Medical Genetics - Neuropsychiatric Genetics |
| Volume | 141 B |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 5 Apr 2006 |
| Externally published | Yes |
Keywords
- Contraction
- Expansion
- Germline
- Huntington's disease (HD)
- Single nucleotide polymorphism (SNP)
- Trinucleotide
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