Prenatal diagnosis in Treacher Collins syndrome using combined linkage analysis and ultrasound imaging

被引:37
作者
Edwards, SJ
Fowlie, A
Cust, MP
Liu, DTY
Young, ID
Dixon, MJ
机构
[1] UNIV MANCHESTER,SCH BIOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
[2] UNIV MANCHESTER,DEPT DENT MED,MANCHESTER M13 9PT,LANCS,ENGLAND
[3] UNIV MANCHESTER,DEPT SURG,MANCHESTER M13 9PT,LANCS,ENGLAND
[4] DERBY CITY GEN HOSP,DEPT OBSTET & GYNAECOL,DERBY,ENGLAND
[5] CITY HOSP NOTTINGHAM,DEPT CLIN GENET,NOTTINGHAM,ENGLAND
基金
英国惠康基金;
关键词
Treacher Collins syndrome; human chromosome 5; prenatal diagnosis;
D O I
10.1136/jmg.33.7.603
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Treacher Collins syndrome is an autosomal dominant disorder of facial development, the features of which include conductive hearing loss and cleft palate. In the current investigation, linkage analysis has been used to make first trimester diagnostic predictions in a pregnancy at high risk of producing an affected child. The results of this analysis predicted that the child would be affected. As predictions of the severity of the disease were not possible, the pregnancy was also assessed by ultrasound imaging. This confirmed the affected diagnosis and predicted that the child would be severely affected.
引用
收藏
页码:603 / 606
页数:4
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