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劳氏综合征:通过晶状体检查识别携带者。

Lowe's syndrome: identification of carriers by lens examination.

作者信息

Gardner R J, Brown N

出版信息

J Med Genet. 1976 Dec;13(6):449-54. doi: 10.1136/jmg.13.6.449.

Abstract

Lens examinations were performed on 7 obligate and 7 possible carriers of the X-linked gene for Lowe's syndrome, and on 117 controls. By quantitatively grading punctate cortical opacities, it was possible to discriminate between the obligate carriers and the controls with a fair degree of confidence. In the age group most important for genetic counselling, that of child bearing, the data are too limited for the derivation of precise estimates, but may, nevertheless, be useful. More such data are needed.

摘要

对7名Lowe综合征X连锁基因的 obligate携带者、7名可能携带者以及117名对照者进行了晶状体检查。通过对点状皮质混浊进行定量分级,能够在一定程度上可靠地区分 obligate携带者和对照者。在对遗传咨询最为重要的育龄年龄组中,数据有限,无法得出精确估计值,但仍可能有用。还需要更多此类数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be93/1013469/7bcc81495741/jmedgene00313-0036-a.jpg

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