Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosis

被引:35
作者
Fryssira, H
Palmer, R
HallidieSmith, KA
Taylor, J
Donnai, D
Reardon, W
机构
[1] INST CHILD HLTH,MOTHERCARE UNIT CLIN GENET & FETAL MED,LONDON WC1N 1EH,ENGLAND
[2] QUEEN ELIZABETH HOSP CHILDREN,REG CYTOGENET LAB,LONDON,ENGLAND
[3] GREAT ORMOND ST HOSP CHILDREN,DEPT CARDIOL,LONDON WC1N 8JA,ENGLAND
[4] ST MARYS HOSP,DEPT MED GENET,MANCHESTER M13 0JH,LANCS,ENGLAND
关键词
FISH; elastin locus; supravalvular aortic stenosis;
D O I
10.1136/jmg.34.4.306
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Both Williams syndrome and isolated supravalvular aortic stenosis (SVAS) are caused by mutations at the elastin locus. Deletion demonstrable by FISH is the hallmark of Williams syndrome, whereas the mutations reported so far in SVAS have been more subtle. FISH positive elastin hemizygosity has not been reported in isolated SVAS. This report records our experience of FISH for elastin deletion in isolated SVAS and specifically reports a patient with non-Williams related SVAS, positive for the elastin deletion by FISH.
引用
收藏
页码:306 / 308
页数:3
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