A HUMAN VASCULAR DISORDER, SUPRAVALVULAR AORTIC-STENOSIS, MAPS TO CHROMOSOME-7

被引:138
作者
EWART, AK
MORRIS, CA
ENSING, GJ
LOKER, J
MOORE, C
LEPPERT, M
KEATING, M
机构
[1] UNIV UTAH, DIV CARDIOL, SALT LAKE CITY, UT 84112 USA
[2] UNIV UTAH, HOWARD HUGHES MED INST, SALT LAKE CITY, UT 84112 USA
[3] UNIV UTAH, ECCLES PROGRAM HUMAN MOLEC BIOL & GENET, SALT LAKE CITY, UT 84112 USA
[4] UNIV NEVADA, SCH MED, DEPT PEDIAT, LAS VEGAS, NV 89102 USA
[5] INDIANA UNIV, SCH MED, DEPT PEDIAT, DIV PEDIAT CARDIOL, INDIANAPOLIS, IN 46202 USA
[6] INDIANA UNIV, SCH MED, DEPT MED & MOLEC GENET, INDIANAPOLIS, IN 46202 USA
关键词
LINKAGE ANALYSIS; ELASTIN; WILLIAMS SYNDROME;
D O I
10.1073/pnas.90.8.3226
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The pathogenesis of vascular disease is unclear, but genetic factors play an important role. In this study we performed linkage analyses in two families with supravalvular aortic stenosis, an inherited vascular disorder that causes narrowing of major arteries and may lead to cardiac overload and failure. DNA markers on the long arm of chromosome 7 (D7S371, D7S395, D7S448, and ELN) were linked to supravalvular aortic stenosis in both families with a combined logarithm of likelihood for linkage (lod score) of 5.9 at the ELN locus. These findings indicate that a gene for supravalvular aortic stenosis is located in the same chromosomal subunit as elastin, which becomes a candidate for the disease gene.
引用
收藏
页码:3226 / 3230
页数:5
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