VARIABILITY OF EXPRESSION IN TUBEROUS SCLEROSIS

被引:57
作者
NORTHRUP, H
WHELESS, JW
BERTIN, TK
LEWIS, RA
机构
[1] UNIV TEXAS,SCH MED,DEPT NEUROL,HOUSTON,TX 77025
[2] UNIV TEXAS,SCH MED,DEPT PEDIAT,HOUSTON,TX 77025
[3] CTR DEMOG & POPULAT GENET,GRAD SCH BIOMED SCI,HOUSTON,TX
[4] BAYLOR COLL MED,DEPT OPHTHALMOL,HOUSTON,TX 77030
[5] BAYLOR COLL MED,DEPT MED,HOUSTON,TX 77030
[6] BAYLOR COLL MED,DEPT PEDIAT,HOUSTON,TX 77030
[7] BAYLOR COLL MED,INST MOLEC GENET,HOUSTON,TX 77030
关键词
D O I
10.1136/jmg.30.1.41
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We present three families in whom a diagnosis of tuberous sclerosis is difficult to secure and we review published reports about similar cases. Tuberous sclerosis has been reported to affect as many as 1 in 9400 subjects in the population. The manifestations of this disease vary not only between but also within families. Currently no reliable method of prenatal diagnosis is available. For these reasons, subjects known to be at 50% risk should be assessed scrupulously to clarify their status. These cases illustrate the difficulties in the clinical diagnosis of tuberous sclerosis and further reinforce the need for a molecular method of determining whether an at risk subject has the disease.
引用
收藏
页码:41 / 43
页数:3
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