Abstract
A cytogenetic study was performed on 4,117 Korean patients referred for
suspected chromosomal abnormalities. Chromosome aberrations were identified in
17.5% of the referred cases. The most common autosomal abnormality was Down
syndrome and Turner syndrome in abnormalities of sex chromosome. The proportions
of different karyotypes in Down syndrome (trisomy 21 92.5%, translocation 5.1%,
mosaic 2.4%) were similar to those reported in other countries. However, it was
different in Turner syndrome (45, X 28.1%, mosaic 50.8%, 46, X, del (Xq) 4.4%,
46, X, i (Xq) 16.7%), in which proportions of mosaics and isochromosome, 46, X,
i(Xq), were higher than those reported in other countries. In structural
chromosome aberrations of autosome, translocation was the most common (43.6%),
and duplication (21.3%), deletion (14.4%), marker chromosome (7.9%) and ring
chromosome (4.0%) followed in order of frequency. Rates of several normal
variant karyotypes were also described. Inversion of chromosome 9 was observed
in 1.7% of total referred cases.