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Molecular genetic analysis of the DiGeorge syndrome among Korean patients with congenital heart disease.

Authors
 Hyangsuk Hur  ;  Yung Jin Kim  ;  Chung Il Noh  ;  Jeong-Wook Seo  ;  Myoung Hee Kim 
Citation
 MOLECULES AND CELLS, Vol.9(1) : 72-77, 1999 
Journal Title
 MOLECULES AND CELLS 
ISSN
 1016-8478 
Issue Date
1999
MeSH
Adolescent ; Child ; Child, Preschool ; Chromosomes, Human, Pair 11/genetics ; DNA Probes/genetics ; DiGeorge Syndrome/genetics* ; Female ; Heart Defects, Congenital/genetics* ; Humans ; In Situ Hybridization, Fluorescence ; Infant ; Male ; Translocation, Genetic/genetics
Abstract
The DiGeorge syndrome (DGS) is a developmental defect of the third and fourth pharyngeal pouches, which is associated with congenital heart defects, hypoparathyroidism, cell-mediated immunodeficiency, velo-pharyngeal insufficiency and craniofacial dysmorphism. The aetiological factor in a great majority of DGS cases is monosomy for the chromosomal region 22q11. To analyze DGS at the molecular level, a new molecular probe (DGCR680) encompassing the ADU balanced translocation breakpoint was prepared. When 13 Korean patients with DGS-type congenital heart disease were analyzed with this probe, 9 turned out to have a deletion at this locus, and all of them except one exhibited a typical facial dysmorphism associated DGS. Though only 9 independent patients were detected to have a deletion at the locus using the commercial probe N25 (D22S75), which maps at about 160 kb from the ADU breakpoint to the telomeric end, results from fluorescence in situ hybridization revealed a deletion in all cases tested at this locus. Two patients who had a deletion at the locus D22S75 but not at DGCR680 did not exhibit any DGS-type facial abnormalities. This result implies that the 680 bp probe covering the ADU translocation breakpoint might be a candidate for a molecular marker that can distinguish a specific phenotype, such as facial features associated with the DiGeorge syndrome. This study also suggested that systematic approaches with several small DNA probes along the DGCR could help to dissect the complex phenotypes associated with the DiGeorge syndrome, such as cardiac defects, abnormal faces, thymic hypoplasia, cleft palate, and hypocalcemia, etc.
Files in This Item:
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Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Anatomy (해부학교실) > 1. Journal Papers
Yonsei Authors
Kim, Myoung Hee(김명희) ORCID logo https://orcid.org/0000-0001-5652-1452
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/172920
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