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先天性内斜视的遗传因素

Heredity in congenital esotropia.

作者信息

Griffin J R, Asano G W, Somers R J, Anderson C E

出版信息

J Am Optom Assoc. 1979 Nov;50(11):1237-42.

PMID:521576
Abstract

As an approach to the problem of familial tendency for congenital esotropia, four families were selected because of proband (index case) who had congenital esotropia. Available family members were evaluated for strabismus and other anomalies of vision. Several possible risk factors were evaluated and the presence of high accommodative convergence-to-accommodation ratio was remarkable. Increased prevalence of congenital esotropia was found among family members as compared to the general population, but with no consistent pattern of Mendelian (single gene) inheritance. These findings are consistent with but not proof of a multifactorial (polygenic and environmental interaction) model. The implication for practicing optometrists is that families with one member affected with congenital esotropia represent a group with increased risk for recurrence.

摘要

作为解决先天性内斜视家族倾向问题的一种方法,选取了四个因先证者(索引病例)患有先天性内斜视的家庭。对现有的家庭成员进行斜视和其他视力异常评估。评估了几种可能的风险因素,其中高调节性集合与调节比率的存在较为显著。与普通人群相比,家庭成员中先天性内斜视的患病率有所增加,但没有孟德尔(单基因)遗传的一致模式。这些发现与多因素(多基因和环境相互作用)模型相符,但并非其证据。对执业验光师的启示是,有一名成员患先天性内斜视的家庭代表复发风险增加的群体。

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