Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities.
case_report · Level V
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- Record sourced from PubMed, PMID 10204857.
- Also identified by PMC identifier 1734321.
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Abstract
Little is known about the mechanism of CGG instability and the time frame of instability early in embryonic development in the fragile X syndrome. Discordant monozygotic twin brothers with the fragile X syndrome could give us insight into the time frame of the instability. We describe monochorionic diamniotic twin brothers with the fragile X syndrome who had different CGG repeats and different mental capacities, whereas the normal mother had a premutation. The more retarded brother had a full mutation in all his cells and no FMR-1 protein expression in lymphocytes, whereas the less retarded brother had 50%/50% mosaicism for a premutation and full mutation and FMR-1 protein expression in 26% of his lymphocytes. The differences in repeat size could have arisen either before or after the time of splitting. The time of splitting in this type of twin is around day 6-7. Given the high percentage of mosaicism, we hypothesise that the instability started before the time of splitting at day 6-7.
Medical subject headings
- Fragile X Syndrome
- Nerve Tissue Proteins
- RNA-Binding Proteins
- Trinucleotide Repeats
- Twins, Monozygotic