Chromosomal analyses of 4,500 cases of the peripheral blood: An experience in a single hospital for 25 years.
10.3345/kjp.2007.50.9.875
- Author:
Hye Eun SEO
1
;
Ji Hye LEE
;
Ji Yoon KIM
;
Dong Ha LEE
;
Heung Kyo LEE
;
Kun Soo LEE
Author Information
1. Department of Pediatrics, Kyungpook National University School of Medicine, Daegu, Korea. kslee@knu.ac.kr
- Publication Type:Original Article
- Keywords:
Cytogenetic analysis;
Chromosomal abnormality
- MeSH:
Adult;
Child;
Chromosome Aberrations;
Cytogenetic Analysis;
Cytogenetics;
Diagnosis;
Down Syndrome;
Genetic Counseling;
Growth and Development;
Gyeongsangbuk-do;
Hope;
Humans;
Incidence;
Infertility;
Karyotype;
Klinefelter Syndrome;
Korea;
Lymphocytes;
Pediatrics;
Sex Chromosomes;
Turner Syndrome
- From:Korean Journal of Pediatrics
2007;50(9):875-881
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Chromosome analysis is important in genetic study and genetic counseling. This study was performed to evaluate the type and incidence of chromosome abnormalities in a single hospital for 25 years. METHODS: Chromosome analyses were performed on peripheral blood lymphocytes, obtained from 4,856 patients with suspected chromosomal aberrations, referred to cytogenetic laboratory in Department of Pediatrics, Kyungpook National University Hospital from May 1981 to October 2005. RESULTS: We analyzed 4,567 cases. Children were 3,014 cases (66.0%) and adult were 1,553 cases (34.0 %). The most common purpose of the chromosomal analysis was growth and developmental abnormality in children and infertility in adults. Total chromosomal aberration rate was 16.9% (770/4,567). Among those cases, the numerical abnormalities were 12.2% (558 cases), the structural abnormalities were 4.1% (187 cases), and others were 0.5% (25 cases). The relative frequencies of autosomal abnormalities were 6.4% (294 cases) in Down syndrome; 0.2% (7 cases) in Edwards syndrome; 0.1% (4 cases) in Patau syndrome; 0.2% (10 cases) in other abnormalities, of sex chromosome, 2.9% (131 cases) in Klinefelter syndrome; 2.2% (99 cases) in Turner syndrome; 0.2% (8 cases) in 47, XXX; 0.1% (3 cases) in 47, XYY. Among the structural abnormalities, translocation was 1.8% (84 cases), inversion was 0.8% (37 cases), deletion was 0.4% (17 cases), and insertion was 0.3% (13 cases), in order of frequency. CONCLUSION: In this study, the type, incidence and distribution of cytogenetic abnormalities by karyotype were reviewed. We hope that our study could be used as a basic information on the diagnosis, treatment and genetic counseling for chromosome abnormalities in Korea.
