The spectrum of 5p deletion in Korean 20 patients with Cri du chat syndrome.
- Author:
Sang Jin PARK
1
;
Sook Ryung KIM
;
Kum Nyeo BAEK
;
Joon No YOON
;
Eun Jeong JEONG
;
Ji Eun KOWN
;
Hyon J KIM
Author Information
1. Department of Medical Genetics, School of Medicine, Ajou University, Suwon, Korea. genetics@kornet.net
- Publication Type:Original Article
- Keywords:
Cri du Chat syndrome;
5p deletion;
Molecular cytogenetics;
Genotype-phenotype correlation;
CGH array;
Fluorescence in situ hybridization
- MeSH:
Centers for Disease Control and Prevention (U.S.);
Cri-du-Chat Syndrome*;
Cytogenetic Analysis;
Cytogenetics;
Diagnosis;
Fluorescence;
Genetic Association Studies;
Genetic Counseling;
Humans;
Hypertelorism;
In Situ Hybridization;
Incidence;
Intellectual Disability;
Karyotype;
Live Birth;
Microcephaly;
Muscle Hypotonia;
Parents;
Phenotype
- From:Journal of Genetic Medicine
2007;4(2):133-141
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Cri-du-Chat syndrome (CdCs) is a rare but clinically recongnizable condition with an estimated incidence of 1:50,000 live births. The clinical characteristics of the syndrome include severe psychomotor and mental retardation, microcephaly, hypertelorism, hypotonia, and slow growth. Also the size of the chromosome 5p deletion ranges were known from the region 5p13 to the terminal region. In this study, we report the spectrum of 5p deletion in Korean 20 pts. with CdCs and genotype-phenotype associations in CdCs. METHODS: In order to delineate genotype-phenotype correlation, molecular cytogenetic studies including GTG banding and clinical characterization were performed on Korean 20 pts with CdCs including parents. CGH array and Fluorescence in situ hybridization (FISH) analysis were used to confirm a terminal deletion karyotype and map more precisely the location of the deletion breakpoint. RESULTS: Molecular analysis of the spectrum of 5p deletion revealed 9 pts (45%) with a del (5)(p14), 7 pts. (35%) a del (5)(p13), 3 pts. (15%) a del (5)(p15.1) and 1 pt. (5%) a del (5)(p15.2) in 20 pts with CdCs. 4(20%)pts were identified to have additional chromosome abnormalites of deficiency and duplication involving chromosomes of 6, 8, 18, & 22. Parental study identified 3 familial case (2 paternal and 1 maternal origin) showing parents being a balanced translocation carrier. And the comparison study of the deletion break points among these 20 pts. with their phenotype has showed the varying clinical pheno-types in the CdCs critical region. CONCLUSION: The characterization of 5p deletion including parental study may help to delineate the genotypephenotype correlation in CdCs. Also these molecular cytogenetic analyses will be able to offer better information for accurate genetic diagnosis in CdCs and further make possible useful genetic counseling in pts. and family.
