Bzdúch V, Halásová E, Masura J
I. detská klinika DFN v Bratislave, Oddelenie klinickej genetiky FN v Bratislave, CSFR.
Bratisl Lek Listy. 1992 Dec;93(12):615-9.
By means of two dimensional echocardiography supravalvular aortic stenosis was diagnosed in two siblings and their cousin. Autosomal dominant transmission with incomplete penetrance or even non-penetrance is assumed to be involved. Somatic stigmatization, typical for Williams' syndrome, failed to be present in the affected children. The reported family provides further evidence that familial supravalvular aortic stenosis and Williams' syndrome are two distinct clinical entities. (Tab. 1, Fig. 3, Ref. 23.)
通过二维超声心动图,在两名兄弟姐妹及其堂兄/妹中诊断出主动脉瓣上狭窄。推测其遗传方式为常染色体显性遗传,存在不完全显性甚至不显性的情况。受影响的儿童未出现威廉姆斯综合征典型的躯体特征。该报道的家族进一步证明,家族性主动脉瓣上狭窄和威廉姆斯综合征是两种不同的临床病症。(表1,图3,参考文献23)